CuAAC: An Efficient Click Chemistry Reaction on ... - ACS Publications

Review pubs.acs.org/acscombsci

CuAAC: An Efficient Click Chemistry Reaction on Solid Phase Vida Castro,*,#,⊥ Hortensia Rodríguez,*,#,⊥,§ and Fernando Albericio*,#,⊥,◊,∥ #

Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology 08028-Barcelona, Spain CIBER-BBN, Networking Centre on Bioengineering, Biomaterials and Nanomedicine, 08028-Barcelona, Spain ◊ Department of Organic Chemistry, University of Barcelona, 08028-Barcelona, Spain § School of Chemistry, Yachay Tech, Yachay City of Knowledge, Urcuqui, Ecuador ∥ School of Chemistry & Physics, University of KwaZulu-Natal, 4001-Durban, South Africa ⊥

ABSTRACT: Click chemistry is an approach that uses efficient and reliable reactions, such as Cu(I)-catalyzed azide−alkyne cycloaddition (CuAAC), to bind two molecular building blocks. CuAAC has broad applications in medicinal chemistry and other fields of chemistry. This review describes the general features and applications of CuAAC in solid-phase synthesis (CuAAC-SP), highlighting the suitability of this kind of reaction for peptides, nucleotides, small molecules, supramolecular structures, and polymers, among others. This versatile reaction is expected to become pivotal for meeting future challenges in solid-phase chemistry. KEYWORDS: Click Chemistry, CuAAC, solid-phase, azide, alkyne

1. INTRODUCTION

2. GENERAL CONSIDERATIONS REGARDING Cu(I)-CATALYZED AZIDE−ALKYNE CYCLOADDITION ON SOLID PHASE (CuAAC-SP) CuAAC is a type of Huisgen1,3-dipolar cycloaddition based on the formation of 1,4-disubstituted [1,2,3]-triazoles between a terminal alkyne and an aliphatic azide in the presence of copper43,44 and is classified as a Click Chemistry reaction.5 Click Chemistry was defined by Sharpless et al.4,5 as any chemical reaction that allows high yields, generates no sideproducts or ones that are easily removed, is stereospecific, gives physiologically stable products, exhibits a large thermodynamic driving force, and has simple reaction conditions. Research into the synthesis of biomolecules via CuAAC-SP has emerged because of the stability of triazole scaffolds against metabolic degradation.4,5 In this Review, we use the terms CuAAC and Click Chemistry interchangeably. In 2001, Meldal et al.25,26 developed a method for preparing 1,4-disubtituted 1,2,3-triazoles using Cu(I) salts as a catalyst for the 1,3-dipolar cycloaddition of terminal alkynes to azides on SP at room temperature using organic solvents such as ACN, THF, DCM, toluene, and DMF. Shortly after and using protic polar solvents such as t-butyl alcohol, ethanol or water, Sharpless et al.27 independently reported the same reaction in solution, naming it CuAAC (Scheme 1). The CuAAC reaction was a breakthrough in triazole chemistry. The reactions of organic azides with terminal alkynes were shown to be accelerated by copper ions and to proceed regioselectively under these conditions, giving the 1,4disubstituted 1,2,3-triazole regioisomer exclusively. The for-

1

In 1963, Merrifield introduced the concept of solid-phase peptide synthesis (SPPS), reporting the first efficient production of a tetrapeptide on a solid matrix, wherein the peptide chain was grown by covalent attachment of one end to the functionalized support. Thanks to Merrifield’s pioneering work, this concept has become a fully established method in peptide synthesis; however, many other known organic reactions have also been applied on solid phase (SP) supports to address synthetic problems and generate new molecular entities.2,3 Click chemistry4,5 promotes the use of organic reactions that allow the connection of two molecular building blocks in a facile, selective, high-yield reaction under mild conditions with few or no byproducts.4,5 Diels−Alder, Michael addition, pyridyl sulfide reaction, oxyme, thiolene, strain-promoted azide−alkyne cycloaaddition (SPAAC), and Cu(I)-catalyzed azide−alkyne cycloaddition (CuAAC) have all been reported as Click reactions.6−24 In the past decade, the CuAAC25−27 has emerged as an efficient alternative in SP to replace amide bonds in peptides28 and to generate amino acid triazole derivatives,29 cyclic peptides,30 nucleotides,31−33 and new resins.34,35 Furthermore, this chemistry has the capacity to promote bioconjugation and peptide ligation, stemming from the properties of the triazole linkage as a peptide mimetic. This Review describes the general features and applications of CuAAC on SP (CuAAC-SP) and reveals the suitability of this kind of reaction for the modification of peptides,36−38 nucleotides,31−33 small molecules,39 supramolecular structures,40,41 and polymers.42 © 2015 American Chemical Society

Received: May 29, 2015 Revised: November 20, 2015 Published: December 11, 2015 1

DOI: 10.1021/acscombsci.5b00087 ACS Comb. Sci. 2016, 18, 1−14

Review

ACS Combinatorial Science

carried out using a Cu(I) source and polar solvents. CuI, CuBr, CuCl, CuBr(PPh3)3, and [Cu(CH3CN)4]PF6 are the most widely used copper sources, whereas DMF, ACN, THF, DCM, H2O, tBuOH, NMP, DMSO, CHCl3, and MeOH are the most frequently used polar solvents. In some cases, a Cu(II) salt, such as CuSO4·5H2O, is used instead of Cu(I) salt, and the addition of a reductive reagent such as sodium ascorbate is required to reduce Cu(II) to Cu(I). These reactions can be carried out with or without a base, with reaction times ranging between 4 and 63 h. The application of microwave radiations between 40 and 60 °C decreases the reaction time considerably. The yield of CuAAC-SP is often reported as quantitative. In many cases, the process has been monitored by IR spectroscopy, tracking the disappearance of the characteristic azide band in the IR spectrum. The broad range of reaction conditions has allowed the production of a great variety of final products via CuAAC-SP (Table 1), thereby revealing the versatility of this kind of reaction and its huge potential. The main variables in CuAAC-SP are the choice of resin, copper catalyst, solvent, and the presence or absence of a base;

Scheme 1. Cu(I)-Catalyzed Azide−Alkyne Cycloaddition (CuAAC)a

a

For CuAAC-SP, either the alkyne or azide are attached to a solidphase support.

mation of the 1,4-disubtituted 1,2,3-triazole ring occurs rapidly in the presence of Cu(I). The cycloaddition product is chemically inert and stable toward redox reactions and it has strong dipole moment of ∼5 D, as shown by experimental studies,5 hydrogen bond accepting capacity, and aromatic character.45 Table 1 summarizes the main features of the reaction. In general, several resins with a broad range of hydrophobicity have been used to prepare compounds such as peptides, peptoids, PNA, and nucleotides. Most of these reactions were Table 1. General Conditions of CuAAC-SPa resin Tenta Gel

PEGA 800 AMCM 2-CTC

Wang

PAM Rink-amide

Cu(I) cat.

Cu (equiv) 0.2 1

DIEA 2′2-bypiridine

CuBrb

1 0.1−2.5 0.3

DIEA, 2,6-lutidine DIEA TBTA DIEA, 2,6-lutidine TBTA DIEA DIEA, 2,6-lutidine DIEA PMDTA DIEA, 2,6-lutidine DIEA DIEA DIEA, HBTU

CuIb [Cu(CH3CN)4]PF6 CuI CuBrb CuSO4·5H2Ob CuBrb CuBrb CuIb CuI CuI CuBr CuSO4·5H2Ob CuIb CuSO4·5H2Ob CuBra [Cu(CH3CN)4]PF6

0.1 1−0.5 1 0.2−0.5 1 2 1.5 0.2−0.5 0.5 0.1−0.5 1.5 1

CuIb MBHA

Merrifield

CPG

tR (h)

base

CuSO4·5H2Ob

CuBrb CuIb CuSO4·5H2Ob CuSO4·5H2O CuI CuBr(PPh3)3 CuSO4·5H2Ob CuSO4·5H2Ob CuSO4·5H2O CuI CuCl

5 1 5 5 2 0.05

TBTA 2,6-lutidine TBTA DIEA, 2,6-lutidine DIEA TBTA, 2,6-lutidine 2,6-lutidine DIEA, 2,6-lutidine piperidine TEA DIEA

16−48 16−72 16 16−48 6 16 2−48 24 20 1−18c 16 −242c

12 24 16 5−16 1c 10−63c 16−36c 0.2−16 0.5−5c 0.5−4c 16 16

0.4−0.5 TBTA 5 1 1

16c 2c 4 16−48 24−72 2

DIEA

final product

ref

peptide peptide glycooligomer resin, peptide, PNA peptide, PNA glycodendrimer, nucleotide PNA PNA, resin peptide, PNA resin peptoid peptide peptide peptoid peptide, peptoid small molecule oligomer oligomer peptide peptide peptide peptide peptide peptide peptoid resin peptide peptide small molec. small molec., S.S. small molec., S.S. nucleotide nucleotide nucleotide PNA PNA

46 47 48 34, 35, 49, 50 51−54 55, 56 57 58, 59 50, 60−62 34, 35 46, 63, 64 65 30 66 67−70 71 72 60 73 74−77 78 79 80 81 82 34, 35 83, 84 85 86 87−97 98, 99 100−108 109−112 113, 114 115 116

Polar solvents were used in the most reactions. bSodium ascorbate was used as Cu(I) stabilizer. cTemperature between 40 and 60 °C or microwave reaction conditions. S.S.: Supramolecular structure. a

2


Review


on SP, using trimethylsilyl azide as diazo-transfer reagent (Table 2, entry 1). Wong et al.125−129 studied the diazo-transfer of aliphatic amines using Cu (II), Ni (II), Zn (II), tetrabutylammonium hydrogen sulfate, or 18-crown-6 as catalysts or additives, and trifluoromethanesulfonyl azide (triflyl azide) as diazo-transfer reagent. In most cases, the latter is prepared in situ by reaction of trifluoromethanesulfonic anhydride and sodium azide (Table 2, entry 2). Diversely substituted [1,2,3]-triazoles were achieved by treating resin-bound 3-amino-2-butenoic acid amides with tosyl azide in the presence of DMF and DIPEA130 (Table 2, entry 3). In 2010, Katritzky et al.131 synthesized the crystalline benzotriazole-1-yl-sulfonyl azide (Table 2, entry 4) as a new stable and widely available diazo-transfer reagent that efficiently provides N-(α-azidoacyl) benzotriazoles with CuSO4·5H2O as copper source. Crystalline 2-ethylimidazole-1-sulfonyl azide (Table 2, entry 5) was designed by Schottenberger et al.132 as a convenient reagent to improve thermal stability for the azidation of electrophilic carbanions. Similarly, Goddard et al.133,134 developed imidazole-1sulfonyl azide hydrochloride (Table 2, entry 6), an affordable and effective diazo-transfer reagent using K2CO3 and MeOH in the presence of CuSO4·5H2O as copper catalyst source.133 This reagent has proven to equal triflyl azide in its capacity as a “diazo donor” to promote the conversion of primary amines into azides and of activated methylene substrates into diazo compounds. However, there are some safety concerns regarding the potential risk of explosion of this reagent. To identify safer-tohandle forms of this compound, several types of imidazole-1sulfonyl azide salts (Table 2, entry 6) were prepared, and their sensitivity to heat, impact, friction, and electrostatic discharge were quantitatively determined. A number of these salts exhibited improved properties and can be considered safer than the aforementioned hydrochloride.134 In addition, Wang et al.135 reported a facile approach to synthesize this diazotransfer reagent by optimizing the procedure to diminish potential risk of explosion. Some reports support the use of this reagent to prompt efficient diazo-transfer reactions, always using polar solvents or aqueous media.136−139 The introduction of azide groups on SP has been accomplished mainly through direct nucleophilic displacement of chloromethyl-derivatized solid supports by the azide ion.87,88,140 Some of these methods are sluggish under the harsh conditions used and they lack reproducibility. To overcome these limitations, a diazo-transfer reaction using trifyl azide (TfN3) was developed to convert amines into azides on SP, allowing the synthesis of azido peptides,141,142 oligonucletides,55 and glycodendrimers.56 However, TfN3 is unstable and potentially explosive and it requires in situ preparation. To avoid this problem, Hansen et al.143 used imidazole-1-sulfonyl azide hydrochloride (ISA.HCl) as a diazotransfer reagent for the efficient preparation of azido peptides on SP. With the aim to generate azide resins, we recently described the application of the ISA·HCl-based diazo-transfer method to a set of four resins covering a broad range of hydrophobicity.35

Table 1 provides an indication of the variables in each category. Both hydrophobic and hydrophilic resins can be used; however, in all cases a polar solvent has been utilized to obtain quantitative results. The copper catalyst is indispensable, and a Cu(I) stabilizer is widely used. Finally, although a base (i.e., DIEA, piperidine, and others) is not imperative, it has been used in most cases to improve performance. To better understand CuAAC-SP, we describe the current understanding of its mechanism and outline various methods used to synthesizing azide reaction partners. Preparation of the terminal alkyne is not included in this review because this group is usually introduced through conventional SP coupling procedures.48 2.1. Cu(I)-Catalyzed Azide−Alkyne Cycloaddition (CuAAC) Mechanism. The last generally accepted mechanism of the CuAAC reaction is shown in Scheme 2.117,118 Scheme 2. Cu(I)-Catalyzed Azide−Alkyne Cycloaddition (CuAAC) Mechanism

While the involvement of two Cu(I) ions in the reaction has been appreciated for some time, a detailed mechanism of this reaction has remained elusive. Worrell et al. recently showed that two Cu(I) atoms of the catalytic complex become equivalent and can scramble,119 but the mode of binding of the azide to the Cu(I) π-complexes has not been demonstrated experimentally. 2.2. Azide Formation. Azides for the CuAAC-SP can be prepared by various methods,120,121 substitution or diazotransfer being those most commonly used. Aliphatic azides are readily accessible by SN2-type substitution with the highly nucleophilic azide ion.121 These azide derivatives have long been appreciated as an important class of compounds (Table 2).122 Sodium azide (Na+·N− = N+ = N−) is the most widely used azide source.123 The diazo-transfer reaction allows the synthesis of organic azides from primary amines using a diazo-transfer reagent (Scheme 3). The most widely used diazo-transfer reagents are shown in Table 2. The procedure is well suited to SP, since side reactions involving the sensitive aliphatic diazonium ions can be circumvented. As an example, Barral et al.124 performed a particularly efficient conversion of aromatic amines into azides

3. Cu(I)-CATALYZED AZIDE−ALKYNE CYCLOADDITION ON SOLID-PHASE (CuAAC-SP) 3.1. History. In 1996, Zaragoza et al.130 published the first synthesis of diversely substituted [1,2,3]-triazoles on a solid 3


Review

ACS Combinatorial Science Table 2. Azide Formation Reagents

Scheme 3. Diazo-Transfer Reaction from Amine to Azide

support through a cyclization. This synthesis was achieved by treating resin-bound 3-amino-2-butenoic acid amides with tosyl azide in the presence of a tertiary amine. A few years later, in 2002, Meldal et al.26 reported the first mild, efficient, and regiospecific copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes into azides on SP, using hydrophilic PEGA 800 and SPOCC resins to obtain diversely 1,4-substituted [1,2,3]-triazoles in peptide backbones or side chains. Given that CuAAC-SP has been successfully introduced in many fields of science, and to gain a better understanding of this topic, we have classified its use with regard to peptides,36−38 nucleotides,31−33 small molecules,39 supramolecular structures,40,41 and polymers,42 thus demonstrating its potential in SP synthesis over the last ten years. 3.2. Peptides. Peptides as drug candidates have some limitations that are related to their aqueous solubility, lipophilicity, H-bond formation, chemical stability, and metabolic stability (proteolytic or enzymatic degradation). Many strategies, including as the introduction of non-natural amino acids, terminal protection, cyclization, and backbone modifications,37,144 have been used to increase the stability of drug candidate peptides The 1,2,3-triazole has attracted increasing attention as a bioisostere of the amide bond of peptides. Tron et al.28 reported the physicochemical properties of 1,2,3-triazole and compared them with the amide bond. The 1,4-disubstituted triazole scaffold shows similarity to a Z-amide bond (Figure 1). This similarity is appreciated by the following features: the distances between substituents; R to R′ are 3.9 Å in amide and 5.0 Å in 1,4-disubstituted 1,2,3-triazole; the lone pair of 3nitrogen mimics that of the carbonyl oxygen of the amide bond (Figure 1, blue remarked); the polarized C(5)-H bond can act as a hydrogen bonding donor, just like the amide N−H bond (Figure 1, red remarked); and the electrophilic and polarized 4-

Figure 1. Structural similarities between Z-amide bond and the 1,4disubstitued 1,2,3-triazole scaffold.

carbon is electronically similar to the carbonyl carbon (Figure 1, green remarked). The overall dipolar moment of the triazole system is larger than that of the amide bond: amide ∼4 D, 1,4disubstituted1,2,3-triazole ∼5 D, and its hydrogen bonding donor and acceptor properties are more marked than those of an amide bond, improve the properties of peptide mimicry.28,145 For instance, SP synthesis of 1,4-disubstituted 1,2,3-triazole via Click Chemistry has been used to replace the amide bond by 1,4-disubstituted 1,2,3-triazoles to form peptidotriazoles,60 peptide mimics, 146 cyclic peptides, 30 and amino acid modifications.29 Additionally, it has also been applied in radiotracer conjugation,147 peptide ligation,52 and bioconjugation.68 Most of these uses promote the introduction of contact groups to enhance affinity or the formation of glycopeptides,148 PEGylated peptides,82 and peptide nucleic acids64 (Figure 2). The replacement of amide bonds by 1,4-disubstituted 1,2,3triazoles on resin was reported in analog formation of peptidomimetics, such as Leu-enkephalin.146 Furthermore, RGD-based peptidomimetics with high activity and selectivity toward αvβ3 and α5β1,149 a matriptase inhibitor mimic and46 a small peptide mimic of the Grb2-SH2 domain respectively,67 were also reported. Furthermore, the formation of 1,2,3-triazoles as a substitute of 3-oxoalkanoic acids on Wang resin,130 the preparation of Nsubstituted histidine and tripeptide analogs from propargylglycine to form peptidotriazoles on PEGA 800 and SPOCC 4


Review


Figure 2. CuAAC on Solid-Phase Peptide Synthesis (SPPS).

resins,26 and the formation of triazolamer (Figure 2, 2a) under different conditions of CuAAC were established.60 A triazole scan of a biologically relevant peptide and its utility for the identification of novel peptidomimetics with improved properties was also achieved via a CuAAC strategy.79 Also, onresin “Click” construction of peptide diphenyl phosphonates has been reported as a valuable method for the rapid diversification of serine protease activity-based probes (ABPs).74 CuAAC-SP has been used as a macrocyclization tool for the formation of triazole scaffold by substituting an amide bond via Click Chemistry. This reaction yielded the following: cyclic peptide mimetic model to optimize PEG based resins,62 cyclic tetra-, penta-, hexa-, and hepta-peptides (Figure 2, 2b),30 as a new family of cyclopeptide cyclo[-Arg-Gly-Asp-Ψ(triazole)Gly-Xaa-] analogs;150 new cyclic RGD and NGR peptide analogs;78 two asymmetrical cyclopeptides (CP1 and CP2);65 side chain to side chain macrocyclization for the synthesis of a series of 21 amino acid helical peptides;49 cyclic peptide C2BL3C based on membrane penetration C2B loop 3 of Syt1;80 cyclic peptidotriazoles derived from the antimicrobial cyclic peptide c(Lys-Lys-Leu-Lys-Lys-Phe-Lys-Lys-Leu-Gln)

(BPC194);83 and a cyclic peptidosteroid via convergent peptide ligation and macrocyclation.47 Head-to-tail oligopeptide cyclodimerization was also reported when precursors containing azide and alkyne groups were exposed to Cu(I) ions on polystyrene supports.73,81 Cyclic lipopeptidotriazoles, which has proven to be a useful approach to improve the antibacterial activity of the parent peptides, as well as to endow them with antifungal properties, were also prepared using CuAAC-SP.84 CuAAC was also used on azidoproline (Azp) (Figure 2, 2c)29 and on Azp-containing collagen model peptides (CMPs) to study their functionality and conformational properties.75,76 Click chemistry was also applied to attach [18F]fluoroalkynes to peptides functionalized with 3-azidopropionic acid (Figure 2, 2d),147 and also to introduce hydrophilic carbohydrate linker moieties into the stabilized BBS (7−14) sequence previously synthesized on Rink-amide resin bearing the (NαHis) Acchelator labeled with 99mTc using the tricarbonyl technique.151 Several peptide sequences, which contained modified aminoacid propargylglicine (Pra), were attached to red-fluorescent tetramethylrhodamine azide (TAMRA) via CuAAC-SP, in order to generate wide range of fluorescent substances,12 thus allowing the identification of cyclic peptidyl inhibitors against 5


Review


Figure 3. CuAAC-SP for the synthesis of nucleotides.

the calcineurin/NFAT interaction through high-throughput screening of one-bead-one-compound libraries.152,153 In addition, this Click Chemistry has been used to produce assembled and scaffolded peptides from peptide and scaffold precursors N-terminally modified with azido and alkyne moieties, respectively, using 2-CTC resin.52 An efficient selfpurifying N-to-C iterative triazole ligation strategy was also applied to the synthesis of a polypeptide with 160 residues on ChemMatrix, PEGA800 and PEGA1900 resins, achieving high purity without the need of chromatographic purification.154 CuAAC-SP was also used as the key step to obtain valuable aminoacyl-(peptidyl)-penicillins, and this reaction showed general applicability and excellent regioselectivity using Wang resin as solid support (Figure 2, 2e).69 Two biotin linkers of different lengths bearing the activated p-(N-propynoylamino) toluic acid (PATA) were incorporated in biotinylated oligopeptides and C-myc peptide both in solution and on a solid support, achieving excellent yields of conversion.68 In this regard, peptides labeled with short-lived positron emitters were synthesized by CuAAC-SP for later use in molecular imaging by positron emission tomography. 85 Another example is peptides loaded with a dendron via CuAAC-SP; these peptide mimotopes are promising candidates as multivalent ligands for antibody B13-DE1 recognition.155

Resins modified by CuAAC-SP for the purpose of peptide synthesis and another applications have been published. We reported on the CuAAC reaction for the preparation of a novel OH-BTL resin (Figure 2, 2i) to circumvent the disadvantages generated by the use of Wang resin in SPPS.34,35 Another modified resin prepared via CuAAC-SP to solid phase organic synthesis (SPOS) was reported, with an outgoing linker after treatment of DBU in the presence of NaI.156 3.3. Peptoids. Peptoids have become an important class of peptide mimics because of their structural and functional properties.157 Examples of peptoids formed via CuAAC-SP include glycosylated peptoids by global on-resin Click glycoconjugation of alkynyl substituted peptoids (Figure 2, 2f).148 Other highly functionalized peptoid oligomers were generated by sequential CuAAC-SP.158 Also, modular synthesis of glycosylated peptoids and polyamines,63 or amphiphilic peptoid transporters used for cell-penetration66 were performed using Rink-amide resin. A focused dipeptide conjugated azidothymidine (AZT) library has been synthesized, and a convenient and efficient CuAAC-SP has been described using Wang resin as solid support.70 Versatile approaches for the efficient synthesis of PEGylated lipo-peptides via CuAAC “Click” conjugation between alkyne-bearing solid-supported lipopeptides and 6


Review


Figure 4. CuAAC-SP for the synthesis of small molecules.

azido-functionalized PEGs was described using polystyrene or TentaGel resins (Figure 2, 2h).82 Most of the studies cited demonstrated the potential of CuAAC in chemical ligation strategies. Other examples of peptoids were described by Zabrodski et al.,157 reporting a fast and efficient incorporation of the pyridine ligands derivatives into N-substituted glycine peptoid oligomers via CuAAC-SP. 3.4. Peptide Nucleic Acid. Concerning peptide nucleic acids (PNAs), organometallic PNA oligomers were synthesized by Click Chemistry on SP through the insertion of ferrocene into PNA oligomers via 1,2,3-triazole formation on PEGA800 resin.159 Azidoferrocene, ethynylferrocene, and DEPA-ferrocene derivatives were introduced into TentaGel resin via Click Chemistry by reaction with PNA trimer conjugates.50 Other organometallic compounds, such as azidomethyl-ruthenocene, and their application via Click Chemistry with PNA oligomers immmobilized on TentaGel resin have also been reported.57 Furthermore, a new azido derivative of 2,2′-dipicolylamine (Dpa) was successfully coupled on SP to a PNA oligomer (H4-pentynoic acid−spacer−spacer−tgca−tgca−tgca−Lys−NH2; spacer (−NH−(CH2)2−O−(CH2)2−O−CH2−CO−) using CuAAC-SP to give Dpa-PNA oligomer.53 Finally, a fluorescent rhenium-containing PNA bioconjugate (Re-PNA) was prepared by means of conjugation of rhenium tricarbonyl complex of a bis(quinoline)-derived ligand (2-azido-N,N-bis((quinolin2-yl)methyl)ethanamine, L−N3), namely, ([Re(CO)3(L− N3)]Br), to a PNA oligomer via CuAAC-SP (TentaGel resin).54

The synthesis of PNA bearing a triazole in place of the amide bond assembled via CuAAC-SP (Rink-amide resin) has been achieved (Figure 2, 2g).64 Click attachment of peptide to oligonucleotides on solid support (Wang resin) was also reported.116 Several peptide-siRNA conjugates were also obtained by a CuAAC-SP strategy, using an alkynyl nucleoside analog “clicked” onto a peptide-derivatized CPG (controlled pore glass) as solid support.115 Finally, fluorescent molecules were attached to pyrrolidinyl peptide nucleic acid bearing a Dprolyl-2-aminocyclopentane carboxylic acid backbone (acpcPNA) as a base surrogate via a triazole linker and using a CuAAC strategy on TentaGel resin as solid support.51,58 3.5. Nucleotides. The structural diversity of active nucleosides proves that nucleoside analogs do not need to resemble their natural counterpart, and these new structures are worth exploring. In this regard, researchers have moved their attention to the possible benefits of innovative and new synthetic approaches, such as CuAAC-SP, for the synthesis of modified nucleosides,31 in which the phosphodiester linkage is replaced by 1,2,3-triazole moiety. This moiety is able to form cyclic nucleotides or assists in bioconjugation, such as in the case of glyconucleotides, glycoclusters,32 and contact groups (Figure 3). To discover new derivatives with potential biological activity, CuAAC-SP has been applied to the loading of alkynefunctionalized leader nucleoside monomers suitable for SP oligonucleotide synthetic applications (Figure 3, 3a).55,160 In relation to the replacement of phosphodiester linkage by 1,2,3triazole moiety, Isobe et al. designed and synthesized a new 7


Review


Figure 5. CuAAC-SP supramolecular structures and polymer applications.

triazole-linked analog of DNA on TentaGel resin (Figure 3, 3b).100 On the other hand, Morvan et al. designed an azido linker to prepare a DNA oligonucleotide, bearing both 3′-azide and 5′alkyne functions on CPG resin. Cycloadditions were performed (Figure 3, 3c).101 CuAAC-SP has also been applied to the synthesis of new nucleoside bioconjugates31 and to the generation of small libraries of nucleoside derivatives on resin.161 Indeed, the efficiency and simplicity of this reaction make it an attractive choice for the covalent linkage of two molecular entities to provide biomolecules with novel properties, such as biological activity, altered hydrophobicity, increased bioaffinity, or the capacity to carry metal ions.31 For instance, glyconucleotides were synthesized by 1,3-dipolar cycloaddition not only of T12trispropargylphosphoramidate oligonucleotide with galactosyl azide on SP (CPG resin)102 but also of manose and galactose-alkyne for the preparation of oligonucleotide conjugates.103 Glycocluster synthesis is carried out using the CPG resin as solid support.104−106 DNA-based glycoclusters can be fucosylated pentaerythityl phosphodiester oligomers (PePOs) (Figure 3, 3d),104 phosphodiester galactosyl clusters,105 or carbohydrate-centered galactosyl clusters.106

Mannose and galactose oligonucleotide conjugates have been prepared by bi-Click Chemistry (two successive CuAACsSP).109 The efficient synthesis of RNA conjugates with nonnucleoside building blocks has been described by Click Chemistry on CPG resin (Figure 3, 3e).110,111,113,162−164 The introduction of contact groups for recognition was also assisted by Click Chemistry. Biotin linker (p-N-propynoylaminotoluic acid, PATA) was conjugated to oligonucleotides.68 The sitespecific incorporation of diamondoids on DNA via CuAAC on CPG resin was achieved (Figure 3, 3f).165 Facile one-step SP synthesis of multitopic organic-DNA hybrids on GPC beads was performed via CuAAC.112 Another example is the use of CuAAC-SP to prepare fluorescent DNA probes containing internal xanthenes and cyanine dyes.114 Meyer et al.107 described the synthesis of heteroglyco 5′-oligonucleotide conjugates via CuAAC-SP with the formation of phosphoramidite derivatives bearing orthogonal function alkyne/thioacetyl, and an azide-bearing carbohydrate. Tähtinen et al.108 reported the synthesis of Neomycinconjugated homopyrimidine oligo 2′-deoxyribonucleotides on SP using Click Chemistry as these compounds are potential therapeutic agents since they recognize the DNA and the double helical RNA. 8


Review


Hartmann et al.48 developed heteromultivalent glycooligomers by CuAAC for application in several fields such as antiviral drugs, vaccines and biosensors.48 The synthesis of molecularly encoded oligomers using a chemoselective CuAAC-SP was also carried out.72 Furthermore, the design and synthesis of a series of solid-tethered rotaxanes utilizing crown ether-naphthalene diimide or crown ether-bipyridinium host guest interactions were described (Figure 5, 5b).59 TentaGel polystyrene resins were initially modified into azide-functionalized beads in a twostage procedure before the target supramolecular architectures were attached.59 The modification of polymers after the successful achievement of polymerization is a central task in macromolecular science.10 CuAAC-SP has been applied to polymeric synthesis. Haddleton et al.99,169 developed the living radical polymerization of methyl methacrylate (MMA) and a fluorescent comonomer with 2-bromo-2-methylpropionic acid 3-azidopropyl ester and 2-bromo-2-methylhept-6-yn-3-ester as initiators. These initiators have been successfully used in the synthesis of fluorescently tagged azide- and alkyne-terminated poly(methyl methacrylate) (PMMA) with average number of molar mass (Mn) close to that predicted, PDI < 1.20, and good first order kinetics, as expected for a living polymerization. Cho et al.96 prepared multiwalled carbon nanotubes (MWCNTs) functionalized with poly(styrene-b-(ethylene-cobutylene)-b-styrene) triblock copolymer (SEBS) using Click Chemistry. In this case, various compositions of SEBSfunctionalized MWCNTs were obtained from the reaction of azide moiety-containing SEBS on styrene units with alkynedecorated MWCNTs (Figure 5, 5c). Girard et al.97 developed the polystyrene-supported triazoles via CuAAC on Merrifield resin. Affinity chromatography is crucial for separating or analyzing specific target compounds in samples and for studying biological interactions. The immobilization of biomolecules is a mainstay in biological fields and related areas, with many potential applications such as the characterization of their functions and their interaction with other biomolecules, the analysis and purification of mixtures of biomolecules, and the design of SP-based assays or bioactive implant surfaces. The CuAAC has been used on silica supports and the modified supports have been successfully applied in affinity chromatography. For instance, the covalent immobilization of suitable alkyne/ azide carbohydrate derivatives on complementarily functionalized azide/alkyne silica was performed by Click ligation through CuAAC reaction of such compounds. New glyco-silicas have shown to be efficient and valuable bioselective affinity chromatographic supports for the purification of lectins, as well as for the one-pot fluorescent labeling of these proteins.170 Yang et al.171 developed a method, namely hydrophilic interaction chromatography (HILIC), which used a support prepared by clicking aspartic acid onto silica gel (termed as Click AA). This material was used as SP extraction sorbent for selective enrichment of glycopeptides.171 Another example reported was the building of 2-oxoglutaric acid receptor attached to resin via CuAAC-SP. This scaffold showed high affinity and specificity to separate the established 2-OG binding protein NtcA.172

3.6. Small Molecules. The combinatorial synthesis of libraries based on the so-called small molecules as bioactive entities has led to increased pressure on chemical synthesis to enhance throughput. SPOS has become an area of huge interest in organic and medicinal chemistry; the application of SPOS comprises a broad variety of organic reactions. For instance, CuAAC is a specific reaction that has been successfully applied on SP for small molecules (Figure 4). Initially, Gmeiner et al.87−92,166 developed an efficient 1,3dipolar cycloaddition of alkynyl-substituted handles with azidomethyl polystyrene that allowed the preparation of the formylaryloxymethyltriazole (FAMT) handle and the formylindolylmethyltriazole linker (FIMT) as backbone amide linker (BAL) analog for the parallel synthesis of pharmacologically tested compounds (Figure 4, 4a), with affinity for selective dopamine D4 receptor ligands.87 The same concept of resin, in this case known as regenerative Michael acceptor (REM) resin, was developed for the synthesis of tertiary amines (Figure 4, 4b).88 Dopamine receptor ligands,89 N-benyltriazolescarboxamides as superpotent G-protein-coupled receptor ligands,90 dopaminergic phenylacetylenes,91 dopamine D4 selective positron emission tomography (PET) ligand candidate (Figure 4, 4c),92 and a potent dopaminergic N-phenyltriazole carboxamides166 were synthesized by CuAAC on SP using polystyrene resin. Moses et al.93 prepared ethynyldiisopropyldilyl as a new silylbased reagent for “catch and release” immobilization, combining Click Chemistry with silyl protection (Figure 4, 4d). In this case, the traditional “all carbon” attachment to solid supports in a silyl-type linker was substituted by a stable triazole, which was easily assembled using the CuAAC reaction on polystyrene resin.93 Nielsen et al.61 developed the synthesis of NH-1,2,3-triazoles, which were prepared by a Click strategy using an acid-labile azido linker supported on PEGA800, polystyrene, TentaGel, ChemMatrix, or Wang resins. An efficient method for the preparation of 1,4-disubstituted 1,2,3-triazole compounds was also described using polymeric quaternary ammonium salts with azide or alkyne functionality to remove unreacted excess starting molecules (azide/ alkyne).86 Click Chemistry was used to build a polyheterocyclicbenzopyran library98 and also to develop a useful kit for the detection of a molecule of interest.167 Furthermore, the synthesis of triazole-based dansylfluorophore for selective and sensitive ratiometric detection of Hg2+ was developed by Lee et al. (Figure 4, 4e)77 on Rink-amide resin. Gothelf et al.168 developed the synthesis of dopamine and serotonin synthesized with short PEG ethers, which were azidefunctionalized to promote coupling onto alkyne-modified magnetic beads (Dynabeads M-270) via Click Chemistry on SP.168 Also, Pericàs et al.94 used the Click strategy to immobilize MacMillan organocatalyst onto polymers and magnetic nanoparticles.94 Portnoy et al. studied one-pot esterification−Click reactions for the functionalization of Wang resin via CuAAC.71 Recently, the SPOS of 1-vinyl and 1-allyl substituted 1,2,3-triazoles was achieved on a selenium linker on solid support via Click Chemistry.95 3.7. Supramolecular Structures and Polymers. CuAAC-SP has been successfully applied to supramolecular structures, polymers, and affinity chromatography fields (Figure 5). The synthesis of lysine-based glycodendrimers as antagonists against Escherichia coli (Figure 5, 5a) using Click Chemistry was carried out by means of azide-functionalized Rink resin and propargyl α-D-mannopiryranoside.56 Moreover,

4. CONCLUSIONS CuAAC has made a significant contribution to Click Chemistry but has also been greatly extended to SP in recent years. This 9


Review


(8) Gil, M.; Arévalo, M.; López, Ó . Click Chemistry - What’s in a Name? Triazole Synthesis and Beyond. Synthesis 2007, 2007, 1589− 1620. (9) Meldal, M. Polymer “Clicking” by CuAAC Reactions. Macromol. Rapid Commun. 2008, 29, 1016−1051. (10) Binder, W. H.; Sachsenhofer, R. Click” Chemistry in Polymer and Materials Science. Macromol. Rapid Commun. 2007, 28, 15−54. (11) Bock, V. D.; Hiemstra, H.; van Maarseveen, J. H. CuI-Catalyzed Alkyne-Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective. Eur. J. Org. Chem. 2006, 2006, 51−68. (12) Hintersteiner, M.; Kimmerlin, T.; Kalthoff, F.; Stoeckli, M.; Garavel, G.; Seifert, J.-M.; Meisner, N.-C.; Uhl, V.; Buehler, C.; Weidemann, T.; Auer, M. Single Bead Labeling Method for Combining Confocal Fluorescence on-Bead Screening and Solution Validation of Tagged One-Bead One-Compound Libraries. Chem. Biol. 2009, 16, 724−735. (13) Jewett, J. C.; Bertozzi, C. R. Cu-Free Click Cycloaddition Reactions in Chemical Biology. Chem. Soc. Rev. 2010, 39, 1272−1279. (14) Moses, J. E.; Moorhouse, A. D. The Growing Applications of Click Chemistry. Chem. Soc. Rev. 2007, 36, 1249−1262. (15) Meldal, M.; Tornøe, C. W. Cu-Catalyzed Azide - Alkyne Cycloaddition. Chem. Rev. 2008, 108, 2952−3015. (16) Hein, J. E.; Fokin, V. V. Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) and beyond: New Reactivity of copper(I) Acetylides. Chem. Soc. Rev. 2010, 39, 1302−1315. (17) Lutz, J.-F. 1,3-Dipolar Cycloadditions of Azides and Alkynes: A Universal Ligation Tool in Polymer and Materials Science. Angew. Chem., Int. Ed. 2007, 46, 1018−1025. (18) Wu, P.; Fokin, V. V. Catalytic Azide-Alkyne Cycloaddition: Reactivity and Applications. Aldrichimica Acta 2007, 40, 7−17. (19) Majumder, N. Click Chemistry in Nano Drug Delivery System and Its Applications in Biology. Int. J. Res. Pharm. Chem. 2015, 5, 95− 105. (20) Paris, C.; Brun, O.; Pedroso, E.; Grandas, A. Exploiting Protected Maleimides to Modify Oligonucleotides, Peptides and Peptide Nucleic Acids. Molecules 2015, 20, 6389−6408. (21) Dar, M. A.; Shrivastava, S.; Iqbal, P. F. Click Chemistry and Anticancer Propierties of 1,2,3-Triazoles. World J. Pharm. Res. 2015, 4, 1949−1975. (22) Totobenazara, J.; Burke, A. J. New Click-Chemistry Methods for 1,2,3-Triazoles Synthesis: Recent Advances and Applications. Tetrahedron Lett. 2015, 56, 2853−2859. (23) Tornøe, C. W.; Meldal, M. Dipolar Cycloaddition Reactions in Peptide Chemistry. In Organic Azides: Syntheses and Applications; Bräse, S., Banert, K., Eds.; John Wiley & Sons, Ltd.: Chichester, United Kingdom, 2010; pp 285−310. (24) Benjamin, R. B.; Heaney, H. Mechanistic Investigations of Copper(I)-Catalysed Alkyne−Azide Cycloaddition Reactions. In Click Triazoles; Košmrlj, J., Ed.; Springer Verlag: Berlin, 2012; pp 1−29. (25) Tornøe, C. W.; Meldal, M. The Wave of the Future; Lebl, M., Houghten, R. A., Eds.; American Petide Society and Kluwer Academic: San Diego, CA, 2001; pp 263−264. (26) Tornøe, C. W.; Christensen, C.; Meldal, M. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(i)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides. J. Org. Chem. 2002, 67, 3057−3064. (27) Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A Stepwise Huisgen Cycloaddition Process: copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes. Angew. Chem., Int. Ed. 2002, 41, 2596−2599. (28) Tron, G. C.; Pirali, T.; Billington, R. A.; Canonico, P. L.; Sorba, G.; Genazzani, A. A. Click Chemistry Reactions in Medicinal Chemistry: Applications of the 1, 3-Dipolar Cycloaddition Between Azides and Alkynes. Med. Res. Rev. 2008, 28, 278−308. (29) Gopi, H. N.; Tirupula, K. C.; Baxter, S.; Ajith, S.; Chaiken, I. M. Click Chemistry on Azidoproline: High-Affinity Dual Antagonist for HIV-1 Envelope Glycoprotein gp120. ChemMedChem 2006, 1, 54−57.

review reveals the potential of this kind of Click reaction for the rapid construction of several molecules. We focused on CuAAC-SP, taking to account the capacity of this method to prepare a wide range of molecular entities, such as peptides, nucleotides, small molecules, supramolecular structures, and polymers. CuAAC-SP has been performed in the presence of the alkyne and the azide (one of them attached to the SP), a Cu(I) source, and the adequate solvent under basic conditions. In most reports either CuI, DIEA, and DMF or CuSO4·5H2O, Asc, and water/tBuOH were the reagents used as copper source, base, and solvent, respectively. CuAAC-SP allowed the replacement of amide bonds in peptides, thus facilitating the synthesis of cyclic or mimetic peptides. In addition to its application in bioconjugation, this reaction has also been used to generate new resins and amino acid-triazole derivatives. Favorable conditions to carry out the CuAAC-SP open up new avenues to tackle future synthetic challenges.

■

AUTHOR INFORMATION

Corresponding Authors

*E-mail: [email protected]. *E-mail: [email protected]. *E-mail: [email protected]. Funding

The work was carried out in the authors’ laboratories. The study was partially funded by the CICYT (CTQ2012-30930), the Generalitat de Catalunya (2014 SGR 137), and the Institute for Research in Biomedicine Barcelona (IRB Barcelona). Notes

The authors declare no competing financial interest.

■

ABBREVIATIONS DMF dimethylformamide; ACN acetonitrile; THF tetrahydrofuran; DCM dichloromethane; NMP N-methylpyrrolidone; DMSO dimethyl sulfoxide; DIEA N,N-diisopropylethylamine; TEA triethylamine; TBTA tris (benzyltriazolylmethyl)amine; PMDTA N,N,N′,N′,N″-pentamethyldiethylenetriamine; CuAAC Cu(I)-catalyzed azide−alkyne cycloaddition; SPOCC (solid-phase organic and combinatorial chemistry) resin; PEGA poly(ethylene glycol) amide backbone resin

■

REFERENCES

(1) Merrifield, R. Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide. J. Am. Chem. Soc. 1963, 85, 2149−2154. (2) Jensen, K. J. Peptide Synthesis. In Pharmaceutical Formulation Development of Peptides and Proteins; Hovgaard, L., Frokjaer, S., van de Weert, M., Eds.; Taylor & Francis: Boca Raton, FL, 2013; pp 1−16. (3) Albericio, F.; Tulla-Puche, J. The Classic Concept of Solid Support. In The Power of Functional Resins in Organic Synthesis; TullaPuche, J., Albericio, F., Eds.; Wiley-VCH Verlag GmbH & Co.: Weinheim, Germany, 2008; pp 3−14. (4) Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click Chemistry: Diverse Chemical Function from a Few Good Reactions. Angew. Chem., Int. Ed. 2001, 40, 2004−2021. (5) Kolb, H. C.; Sharpless, K. B. The Growing Impact of Click Chemistry on Drug Discovery. Drug Discovery Today 2003, 8, 1128− 1137. (6) Liang, L.; Astruc, D. The copper(I)-Catalyzed Alkyne-Azide Cycloaddition (CuAAC) “Click” Reaction and Its Applications. An Overview. Coord. Chem. Rev. 2011, 255, 2933−2945. (7) Jawalekar, A. M.; Malik, S.; Verkade, J. M. M.; Gibson, B.; Barta, N. S.; Hodges, J. C.; Rowan, A.; van Delft, F. L. Oligonucleotide Tagging for Copper-Free Click Conjugation. Molecules 2013, 18, 7346−7363. 10


Review

ACS Combinatorial Science (30) Turner, R. A.; Oliver, A. G.; Lokey, R. S. Click Chemistry as a Macrocyclization Tool in the Solid-Phase Synthesis of Small Cyclic Peptides. Org. Lett. 2007, 9, 5011−5014. (31) Amblard, F.; Cho, J. H.; Schinazi, R. F. Cu(I)-Catalyzed Huisgen Azide-Alkyne 1,3-Dipolar Cycloaddition Reaction in Nucleoside, Nucleotide, and Oligonucleotide Chemistry. Chem. Rev. 2009, 109, 4207−4220. (32) Morvan, F.; Vidal, S.; Souteyrand, E.; Chevolot, Y.; Vasseur, J.-J. DNA Glycoclusters and DNA-Based Carbohydrate Microarrays: From Design to Applications. RSC Adv. 2012, 2, 12043−12068. (33) Abramova, T. Frontiers and Approaches to Chemical Synthesis of Oligodeoxyribonucleotides. Molecules 2013, 18, 1063−1075. (34) Castro, V.; Rodriguez, H.; Albericio, F. Wang Linker Free of Side Reactions. Org. Lett. 2013, 15, 246−249. (35) Castro, V.; Blanco-Canosa, J. B.; Rodriguez, H.; Albericio, F. Imidazole-1-Sulfonyl Azide-Based Diazo-Transfer Reaction for the Preparation of Azido Solid Supports for Solid-Phase Synthesis. ACS Comb. Sci. 2013, 15, 331−334. (36) Meldal, M.; Tornøe, C. W.; Nielsen, T. E.; Diness, F.; Le Quement, S. T.; Christensen, C. a; Jensen, J. F.; Worm-Leonhard, K.; Groth, T.; Bouakaz, L.; Wu, B.; Hagel, G.; Keinicke, L. Ralph F. Hirschmann Award Address 2009: Merger of Organic Chemistry with Peptide Diversity. Biopolymers 2010, 94, 161−182. (37) Li, H.; Aneja, R.; Chaiken, I. Click Chemistry in Peptide-Based Drug Design. Molecules 2013, 18, 9797−9817. (38) Chandrudu, S.; Simerska, P.; Toth, I. Chemical Methods for Peptide and Protein Production. Molecules 2013, 18, 4373−4388. (39) Millward, S. W.; Agnew, H. D.; Lai, B.; Lee, S. S.; Lim, J.; Nag, A.; Pitram, S.; Rohde, R.; Heath, J. R. In Situ Click Chemistry: From Small Molecule Discovery to Synthetic Antibodies. Integr. Biol. 2013, 5, 87−95. (40) Avti, P. K.; Maysinger, D.; Kakkar, A. Alkyne-Azide “Click” Chemistry in Designing Nanocarriers for Applications in Biology. Molecules 2013, 18, 9531−9549. (41) Pasini, D. The Click Reaction as an Efficient Tool for the Construction of Macrocyclic Structures. Molecules 2013, 18, 9512− 9530. (42) Wong, C.-H.; Zimmerman, S. C. Orthogonality in Organic, Polymer, and Supramolecular Chemistry: From Merrifield to Click Chemistry. Chem. Commun. (Cambridge, U. K.) 2013, 49, 1679−1695. (43) Huisgen, R. 1,3-Dipolar Cycloadditions. Past and Future. Angew. Chem., Int. Ed. Engl. 1963, 2, 565−598. (44) Sustmann, R. Rolf Huisgen’s Contribution to Organic Chemistry, Emphasis 1,3-Dipolar Cycloadditions. Heterocycles 1995, 40, 1−18. (45) Himo, F.; Lovell, T.; Hilgraf, R.; Rostovtsev, V. V.; Noodleman, L.; Sharpless, K. B.; Fokin, V. V. Copper(I)-Catalyzed Synthesis of Azoles. DFT Study Predicts Unprecedented Reactivity and Intermediates. J. Am. Chem. Soc. 2005, 127, 210−216. (46) Fittler, H.; Avrutina, O.; Glotzbach, B.; Empting, M.; Kolmar, H. Combinatorial Tuning of Peptidic Drug Candidates: High-Affinity Matriptase Inhibitors through Incremental Structure-Guided Optimization. Org. Biomol. Chem. 2013, 11, 1848−1857. (47) Clemmen, A.; Boutton, C.; Vanlandschoot, P.; Wittelsberger, A.; Borghmans, I.; Coppens, A.; Casteels, P.; Madder, A. Straightforward Synthesis of Cholic Acid Stabilized Loop Mimetics. Tetrahedron Lett. 2014, 55, 423−429. (48) Ponader, D.; Maffre, P.; Aretz, J.; Pussak, D.; Ninnemann, N. M.; Schmidt, S.; Seeberger, P. H.; Rademacher, C.; Nienhaus, G. U.; Hartmann, L. Carbohydrate-Lectin Recognition of Sequence-Defined Heteromultivalent Glycooligomers. J. Am. Chem. Soc. 2014, 136, 2008−2016. (49) Ingale, S.; Dawson, P. E. On Resin Side-Chain Cyclization of Complex Peptides Using CuAAC. Org. Lett. 2011, 13, 2822−2825. (50) Hüsken, N.; Gasser, G.; Köster, S. D.; Metzler-Nolte, N. FourPotential” Ferrocene Labeling of PNA Oligomers via Click Chemistry. Bioconjugate Chem. 2009, 20, 1578−1586. (51) Mansawat, W.; Boonlua, C.; Siriwong, K.; Vilaivan, T. Clicked Polycyclic Aromatic Hydrocarbon as a Hybridization-Responsive

Fluorescent Artificial Nucleobase in Pyrrolidinyl Peptide Nucleic Acids. Tetrahedron 2012, 68, 3988−3995. (52) Franke, R.; Doll, C.; Eichler, J. Peptide Ligation through Click Chemistry for the Generation of Assembled and Scaffolded Peptides. Tetrahedron Lett. 2005, 46, 4479−4482. (53) Gasser, G.; Jäger, K.; Zenker, M.; Bergmann, R.; Steinbach, J.; Stephan, H.; Metzler-Nolte, N. Preparation, 99mTc-Labeling and Biodistribution Studies of a PNA Oligomer Containing a New Ligand Derivative of 2,2′-Dipicolylamine. J. Inorg. Biochem. 2010, 104, 1133− 1140. (54) Gasser, G.; Pinto, A.; Neumann, S.; Sosniak, A. M.; Seitz, M.; Merz, K.; Heumann, R.; Metzler-Nolte, N. Synthesis, Characterisation and Bioimaging of a Fluorescent Rhenium-Containing PNA Bioconjugate. Dalt. Trans. 2012, 41, 2304−2313. (55) Oyelere, A. K.; Chen, P. C.; Yao, L. P.; Boguslavsky, N. Heterogeneous Diazo-Transfer Reaction: A Facile Unmasking of Azide Groups on Amine-Functionalized Insoluble Supports for Solid-Phase Synthesis. J. Org. Chem. 2006, 71, 9791−9796. (56) Papadopoulos, A.; Shiao, T. C.; Roy, R. Diazo Transfer and Click Chemistry in the Solid Phase Syntheses of Lysine-Based Glycodendrimers as Antagonists against Escherichia Coli FimH. Mol. Pharmaceutics 2012, 9, 394−403. (57) Patra, M.; Metzler-Nolte, N. Azidomethyl-Ruthenocene: Facile Synthesis of a Useful Metallocene Derivative and Its Application in the “Click” Labelling of Biomolecules. Chem. Commun. (Cambridge, U. K.) 2011, 47, 11444−11446. (58) Ditmangklo, B.; Boonlua, C.; Suparpprom, C.; Vilaivan, T. Reductive Alkylation and Sequential Reductive Alkylation-Click Chemistry for On-Solid-Support Modification of Pyrrolidinyl Peptide Nucleic Acid. Bioconjugate Chem. 2013, 24, 614−625. (59) Wilson, H.; Byrne, S.; Bampos, N.; Mullen, K. M. Click” Functionalised Polymer Resins: A New Approach to the Synthesis of Surface Attached Bipyridinium and Naphthalene Diimide [2]rotaxanes. Org. Biomol. Chem. 2013, 11, 2105−2115. (60) Angelo, N. G.; Arora, P. S. Solution- and Solid-Phase Synthesis of Triazole Oligomers That Display Protein-like Functionality. J. Org. Chem. 2007, 72, 7963−7967. (61) Cohrt, A. E.; Jensen, J. F.; Nielsen, T. E. Traceless Azido Linker for the Solid-Phase Synthesis of NH-1,2,3-Triazoles via Cu-Catalyzed Azide-Alkyne Cycloaddition Reactions. Org. Lett. 2010, 12, 5414− 5417. (62) Roice, M.; Johannsen, I.; Meldal, M. High Capacity Poly(ethylene Glycol) Based Amino Polymers for Peptide and Organic Synthesis. QSAR Comb. Sci. 2004, 23, 662−673. (63) Fürniss, D.; Mack, T.; Hahn, F.; Vollrath, S. B. L.; Koroniak, K.; Schepers, U.; Bräse, S. Peptoids and Polyamines Going Sweet: Modular Synthesis of Glycosylated Peptoids and Polyamines Using Click Chemistry. Beilstein J. Org. Chem. 2013, 9, 56−63. (64) Chouikhi, D.; Barluenga, S.; Winssinger, N. Clickable Peptide Nucleic Acids (cPNA) with Tunable Affinity. Chem. Commun. (Cambridge, U. K.) 2010, 46, 5476−5478. (65) Qin, S.-Y.; Xu, X.-D.; Chen, C.-S.; Chen, J.-X.; Li, Z.-Y.; Zhuo, R.-X.; Zhang, X.-Z. Supramolecular Architectures Self-Assembled from Asymmetrical Hetero Cyclopeptides. Macromol. Rapid Commun. 2011, 32, 758−764. (66) Vollrath, S. B. L.; Fürniss, D.; Schepers, U.; Bräse, S. Amphiphilic Peptoid Transporters-Synthesis and Evaluation. Org. Biomol. Chem. 2013, 11, 8197−8201. (67) Iwata, T.; Tanaka, K.; Tahara, T.; Nozaki, S.; Onoe, H.; Watanabe, Y.; Fukase, K. A Conformationally Fixed Analog of the Peptide Mimic Grb2-SH2 Domain: Synthesis and Evaluation against the A431 Cancer Cell. Mol. BioSyst. 2013, 9, 1019−1025. (68) Jezowska, M.; Romanowska, J.; Bestas, B.; Tedebark, U.; Honcharenko, M. Synthesis of Biotin Linkers with the Activated Triple Bond Donor [p-(N-Propynoylamino)toluic Acid] (PATA) for Efficient Biotinylation of Peptides and Oligonucleotides. Molecules 2012, 17, 14174−14185. 11


Review


Taking Advantage of a Click Chemistry Based BAL Linker. J. Comb. Chem. 2005, 7, 309−316. (90) Loaiza, P. R.; Löber, S.; Hübner, H.; Gmeiner, P. Click Chemistry on Solid Phase: Parallel Synthesis of N-Benzyltriazole Carboxamides as Super-Potent G-Protein Coupled Receptor Ligands. J. Comb. Chem. 2006, 8, 252−261. (91) Rodriguez Loaiza, P.; Löber, S.; Hübner, H.; Gmeiner, P. Click Chemistry Based Solid Phase Supported Synthesis of Dopaminergic Phenylacetylenes. Bioorg. Med. Chem. 2007, 15, 7248−7257. (92) Tietze, R.; Löber, S.; Hübner, H.; Gmeiner, P.; Kuwert, T.; Prante, O. Discovery of a Dopamine D4 Selective PET Ligand Candidate Taking Advantage of a Click Chemistry Based REM Linker. Bioorg. Med. Chem. Lett. 2008, 18, 983−988. (93) Sharma, P.; Moses, J. E. Ethynyldiisopropylsilyl: A New Alkynylsilane Protecting Group and “Click” Linker. Org. Lett. 2010, 12, 2860−2863. (94) Riente, P.; Yadav, J.; Pericàs, M. A Click Strategy for the Immobilization of MacMillan Organocatalysts onto Polymers and Magnetic Nanoparticles. Org. Lett. 2012, 14, 3668−3671. (95) Wang, Q.-Y.; Sheng, W.-S.; Sheng, S.-R.; Li, Y.; Cai, M.-Z. Click Chemistry on Polymer Support: Synthesis of 1-Vinyl- and 1-Allyl1,2,3-Triazoles via Selenium Linker. Synth. Commun. 2014, 44, 59−67. (96) Yadav, S. K.; Mahapatra, S. S.; Cho, J. W.; Lee, J. Y. Functionalization of Multiwalled Carbon Nanotubes with Poly (styrene-B-(ethylene-Co-Butylene)-B-Styrene) by Click Coupling. J. Phys. Chem. C 2010, 114, 11395−11400. (97) Ouerghui, A.; Elamari, H.; Ghammouri, S.; Slimi, R.; Meganem, F.; Girard, C. Polystyrene-Supported Triazoles for Metal Ions Extraction: Synthesis and Evaluation. React. Funct. Polym. 2014, 74, 37−45. (98) Zhu, M.; Lim, B. J.; Koh, M.; Park, S. B. Construction of Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway. ACS Comb. Sci. 2012, 14, 124−134. (99) Chen, G.; Tao, L.; Mantovani, G.; Ladmiral, V.; Burt, D. P.; Macpherson, J. V.; Haddleton, D. M. Synthesis of Azide/alkyneTerminal Polymers and Application for Surface Functionalisation through a [2 + 3] Huisgen Cycloaddition Process, “Click Chemistry. Soft Matter 2007, 3, 732−739. (100) Isobe, H.; Fujino, T.; Yamazaki, N.; Guillot-Nieckowski, M.; Nakamura, E. Triazole-Linked Analogue of Deoxyribonucleic Acid ((TL)DNA): Design, Synthesis, and Double-Strand Formation with Natural DNA. Org. Lett. 2008, 10, 3729−3732. (101) Pourceau, G.; Meyer, A.; Vasseur, J.-J.; Morvan, F. Azide Solid Support for 3′-Conjugation of Oligonucleotides and Their Circularization by Click Chemistry. J. Org. Chem. 2009, 74, 6837−6842. (102) Bouillon, C.; Meyer, A.; Vidal, S.; Jochum, A.; Chevolot, Y.; Cloarec, J.; Praly, J.; Vasseur, J.; Morvan, F. Microwave Assisted “ Click ” Chemistry for the Synthesis of Multiple Labeled-Carbohydrate Oligonucleotides on Solid Support. J. Org. Chem. 2006, 71, 4700− 4702. (103) Pourceau, G.; Meyer, A.; Vasseur, J.-J.; Morvan, F. Synthesis of Mannose and Galactose Oligonucleotide Conjugates by Bi-Click Chemistry. J. Org. Chem. 2009, 74, 1218−1222. (104) Morvan, F.; Meyer, A.; Jochum, A.; Sabin, C.; Chevolot, Y.; Imberty, A.; Praly, J.-P.; Vasseur, J.-J.; Souteyrand, E.; Vidal, S. Fucosylated Pentaerythrityl Phosphodiester Oligomers (PePOs): Automated Synthesis of DNA-Based Glycoclusters and Binding to Pseudomonas Aeruginosa Lectin (PA-IIL). Bioconjugate Chem. 2007, 18, 1637−1643. (105) Pourceau, G.; Meyer, A.; Vasseur, J.-J.; Morvan, F. Combinatorial and Automated Synthesis of Phosphodiester Galactosyl Cluster on Solid Support by Click Chemistry Assisted by Microwaves. J. Org. Chem. 2008, 73, 6014−6017. (106) Pourceau, G.; Meyer, A.; Chevolot, Y.; Souteyrand, E.; Vasseur, J.-J.; Morvan, F. Oligonucleotide Carbohydrate-Centered Galactosyl Cluster Conjugates Synthesized by Click and Phosphoramidite Chemistries. Bioconjugate Chem. 2010, 21, 1520−1529.

(69) Cornier, P. G.; Boggián, D. B.; Mata, E. G.; Delpiccolo, C. M. L. Solid-Phase Based Synthesis of Biologically Promising Triazolyl Aminoacyl (peptidyl) Penicillins. Tetrahedron Lett. 2012, 53, 632−636. (70) Zhang, L.; Zhang, L.; Luo, T.; Zhou, J.; Sun, L.; Xu, Y. Synthesis and Evaluation of a Dipeptide-Drug Conjugate Library as Substrates for PEPT1. ACS Comb. Sci. 2012, 14, 108−114. (71) Eppel, S.; Portnoy, M. One-Pot Esterification-Click (CuAAC) and Esterification−acetylene Coupling (Glaser/Eglinton) for Functionalization of Wang Polystyrene Resin. Tetrahedron Lett. 2013, 54, 5056−5060. (72) Trinh, T. T.; Oswald, L.; Chan-Seng, D.; Lutz, J.-F. Synthesis of Molecularly Encoded Oligomers Using a Chemoselective “AB + CD” Iterative Approach. Macromol. Rapid Commun. 2014, 35, 141−145. (73) Punna, S.; Kuzelka, J.; Wang, Q.; Finn, M. G. Head-to-Tail Peptide Cyclodimerization by Copper-Catalyzed Azide-Alkyne Cycloaddition. Angew. Chem., Int. Ed. 2005, 44, 2215−2220. (74) Serim, S.; Mayer, S. V.; Verhelst, S. H. L. Tuning Activity-Based Probe Selectivity for Serine Proteases by on-Resin “Click” Construction of Peptide Diphenyl Phosphonates. Org. Biomol. Chem. 2013, 11, 5714−5721. (75) Erdmann, R. S.; Wennemers, H. Functionalizable Collagen Model Peptides. J. Am. Chem. Soc. 2010, 132, 13957−13959. (76) Erdmann, R. S.; Wennemers, H. Conformational Stability of Triazolyl Functionalized Collagen Triple Helices. Bioorg. Med. Chem. 2013, 21, 3565−3568. (77) Neupane, L. N.; Kim, J. M.; Lohani, C. R.; Lee, K.-H. Selective and Sensitive Ratiometric Detection of Hg2+ in 100% Aqueous Solution with Triazole-Based Dansyl Probe. J. Mater. Chem. 2012, 22, 4003−4008. (78) Metaferia, B. B.; Rittler, M.; Gheeya, J. S.; Lee, A.; Hempel, H.; Plaza, A.; Stetler-Stevenson, W. G.; Bewley, C. a; Khan, J. Synthesis of Novel Cyclic NGR/RGD Peptide Analogs via on Resin Click Chemistry. Bioorg. Med. Chem. Lett. 2010, 20, 7337−7340. (79) Valverde, I. E.; Bauman, A.; Kluba, C. A.; Vomstein, S.; Walter, M. A.; Mindt, T. L. 1,2,3-Triazoles as Amide Bond Mimics: Triazole Scan Yields Protease-Resistant Peptidomimetics for Tumor Targeting. Angew. Chem., Int. Ed. 2013, 52, 8957−8960. (80) Saludes, J. P.; Morton, L. A.; Ghosh, N.; Beninson, L. A.; Chapman, E. R.; Fleshner, M.; Yin, H. Detection of Highly Curved Membrane Surfaces Using a Cyclic Peptide Derived from Synaptotagmin-I. ACS Chem. Biol. 2012, 7, 1629−1635. (81) Jagasia, R.; Holub, J. M.; Bollinger, M.; Kirshenbaum, K.; Finn, M. G. Peptide Cyclization and Cyclodimerization by Cu(I)-Mediated Azide-Alkyne Cycloaddition. J. Org. Chem. 2009, 74, 2964−2974. (82) Jølck, R. I.; Berg, R. H.; Andresen, T. L. Solid-Phase Synthesis of PEGylated Lipopeptides Using Click Chemistry. Bioconjugate Chem. 2010, 21, 807−810. (83) Güell, I.; Vilà, S.; Micaló, L.; Badosa, E.; Montesinos, E.; Planas, M.; Feliu, L. Synthesis of Cyclic Peptidotriazoles with Activity Against Phytopathogenic Bacteria. Eur. J. Org. Chem. 2013, 2013, 4933−4943. (84) Vilà, S.; Camó, C.; Figueras, E.; Badosa, E.; Montesinos, E.; Planas, M.; Feliu, L. Solid-Phase Synthesis of Cyclic Lipopeptidotriazoles. Eur. J. Org. Chem. 2014, 2014, 4785−4794. (85) Pretze, M.; Mosch, B.; Bergmann, R.; Steinbach, J.; Pietzsch, J.; Mamat, C. Radiofluorination and First Radiopharmacological Characterization of a SWLAY Peptide-Based Ligand Targeting EphA2. J. Labelled Compd. Radiopharm. 2014, 57, 660−665. (86) Sirion, U.; Lee, J.-H.; Bae, Y.-J.; Kim, H.-J.; Lee, B.-S.; Chi, D.-Y. Azide/Alkyne Resins for Quick Preparation of 1,4-Disubstituted 1,2,3Triazoles. Bull. Korean Chem. Soc. 2010, 31, 1843−1847. (87) Löber, S.; Rodriguez-Loaiza, P.; Gmeiner, P. Click Linker: Efficient and High-Yielding Synthesis of a New Family of SPOS Resins by 1,3-Dipolar Cycloaddition. Org. Lett. 2003, 5, 1753−1755. (88) Löber, S.; Gmeiner, P. Click Chemistry on Solid Support: Synthesis of a New REM Resin and Application for the Preparation of Tertiary Amines. Tetrahedron 2004, 60, 8699−8702. (89) Bettinetti, L.; Löber, S.; Hübner, H.; Gmeiner, P. Parallel Synthesis and Biological Screening of Dopamine Receptor Ligands 12


Review

ACS Combinatorial Science (107) Meyer, A.; Noël, M.; Vasseur, J.-J.; Morvan, F. Hetero-Click Conjugation of Oligonucleotides with Glycosides Using Bifunctional Phosphoramidites. Eur. J. Org. Chem. 2015, 2015, 2921−2927. (108) Tähtinen, V.; Granqvist, L.; Virta, P. Synthesis of C-5, C-2′ and C-4′-Neomycin-Conjugated Triplex Forming Oligonucleotides and Their Affinity to DNA-Duplexes. Bioorg. Med. Chem. 2015, 23, 4472− 4480. (109) Kiviniemi, A.; Virta, P.; Lonnberg, H. Solid-Supported Synthesis and Click Conjugation of 4 ′- C-Alkyne Functionalized Oligodeoxyribonucleotides. Bioconjugate Chem. 2010, 21, 1890−1901. (110) Jayaprakash, K. N.; Peng, C. G.; Butler, D.; Varghese, J. P.; Maier, M. A.; Rajeev, K. G.; Manoharan, M. Non-Nucleoside Building Blocks for Copper-Assisted and Copper-Free Click Chemistry for the Efficient Synthesis of RNA Conjugates. Org. Lett. 2010, 12, 5410− 5413. (111) Kiviniemi, A.; Virta, P.; Drenichev, M. S.; Mikhailov, S. N.; Lönnberg, H. Solid-Supported 2′-O-Glycoconjugation of Oligonucleotides by Azidation and Click Reactions. Bioconjugate Chem. 2011, 22, 1249−1255. (112) Thaner, R. V.; Eryazici, I.; Farha, O. K.; Mirkin, C. A.; Nguyen, S. T. Facile One-Step Solid-Phase Synthesis of Multitopic organic− DNA Hybrids via “Click” Chemistry. Chem. Sci. 2014, 5, 1091−1096. (113) Ligeour, C.; Meyer, A.; Vasseur, J.-J.; Morvan, F. Bis- and TrisAlkyne Phosphoramidites for Multiple 5′-Labeling of Oligonucleotides by Click Chemistry. Eur. J. Org. Chem. 2012, 2012, 1851−1856. (114) Astakhova, I. K.; Wengel, J. Interfacing Click Chemistry with Automated Oligonucleotide Synthesis for the Preparation of Fluorescent DNA Probes Containing Internal Xanthene and Cyanine Dyes. Chem. - Eur. J. 2013, 19, 1112−1122. (115) Liu, Y.; Wang, X.-F.; Chen, Y.; Zhang, L.-H.; Yang, Z.-J. A Solid-Phase Method for peptide−siRNA Covalent Conjugates Based on Click Chemistry. MedChemComm 2012, 3, 506−511. (116) Wenska, M.; Alvira, M.; Steunenberg, P.; Stenberg, A.; Murtola, M.; Strömberg, R. An Activated Triple Bond Linker Enables “Click” Attachment of Peptides to Oligonucleotides on Solid Support. Nucleic Acids Res. 2011, 39, 9047−9059. (117) Schoffelen, S.; Meldal, M. Alkyne−Azide Reactions. In Modern Alkyne Chemsitry: Catalytic and Atom-Economic Transformations; Trost, B. M., Li, C.-J., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA.: Weinheim, Germany, 2015; Vol. 1, pp 115−142. (118) Ö tvös, S. B.; Georgiádes, Á .; Á dok-Sipiczki, M.; Mészáros, R.; Pálinkó, I.; Sipos, P.; Fülöp, F. A Layered Double Hydroxide, a Synthetically Useful Heterogeneous Catalyst for Azide−alkyne Cycloadditions in a Continuous-Flow Reactor. Appl. Catal., A 2015, 501, 63−73. (119) Worrell, B. T.; Malik, J. A.; Fokin, V. V. Direct Evidence of a Dinuclear Copper Intermediate in Cu(I)-Catalyzed Azide-Alkyne Cycloadditions. Science 2013, 340, 457−460. (120) Scriven, E. F.; Turnbull, K. Azides: Their Preparation and Synthetic Uses. Chem. Rev. 1988, 88, 297−368. (121) Bräse, S.; Gil, C.; Knepper, K.; Zimmermann, V. Organic Azides: An Exploding Diversity of a Unique Class of Compounds. Angew. Chem., Int. Ed. 2005, 44, 5188−5240. (122) L'Abbé, G. Decomposition and Addition Reactions of Organic Azides. Chem. Rev. 1969, 69, 345−363. (123) Le Chevalier Isaad, A.; Barbetti, F.; Rovero, P.; D'Ursi, A. M.; Chelli, M.; Chorev, M.; Papini, A. M. N A -Fmoc-Protected Ω-Azidoand Ω-Alkynyl-L-Amino Acids as Building Blocks for the Synthesis of “Clickable” Peptides. Eur. J. Org. Chem. 2008, 2008, 5308−5314. (124) Barral, K.; Moorhouse, A. D.; Moses, J. E. Efficient Conversion of Aromatic Amines into Azides: A One-Pot Synthesis of Triazole Linkages. Org. Lett. 2007, 9, 1809−1811. (125) Alper, P. B.; Hung, S.-C.; Wong, C.-H. Metal Catalyzed Diazo Transfer for the Synthesis of Azides from Amines. Tetrahedron Lett. 1996, 37, 6029−6032. (126) Yan, R.-B.; Yang, F.; Wu, Y.; Zhang, L.-H.; Ye, X.-S. An Efficient and Improved Procedure for Preparation of Triflyl Azide and Application in Catalytic Diazotransfer Reaction. Tetrahedron Lett. 2005, 46, 8993−8995.

(127) Titz, A.; Radic, Z.; Schwardt, O.; Ernst, B. A Safe and Convenient Method for the Preparation of Triflyl Azide, and Its Use in Diazo Transfer Reactions to Primary Amines. Tetrahedron Lett. 2006, 47, 2383−2385. (128) Beckmann, H. S. G.; Wittmann, V. One-Pot Procedure for Diazo Transfer and Azide-Alkyne Cycloaddition: Triazole Linkages from Amines. Org. Lett. 2007, 9, 1−4. (129) Nyffeler, P. T.; Liang, C.-H.; Koeller, K. M.; Wong, C.-H. The Chemistry of Amine-Azide Interconversion: Catalytic Diazotransfer and Regioselective Azide Reduction. J. Am. Chem. Soc. 2002, 124, 10773−10778. (130) Zaragoza, F.; Petersen, S. V. Solid-Phase Synthesis of Substituted 1,2,3-Triazoles. Tetrahedron 1996, 52, 10823−10826. (131) Katritzky, A. R.; El Khatib, M.; Bol’shakov, O.; Khelashvili, L.; Steel, P. J. Benzotriazol-1-Yl-Sulfonyl Azide for Diazotransfer and Preparation of Azidoacylbenzotriazoles. J. Org. Chem. 2010, 75, 6532− 6539. (132) Laus, G.; Adamer, V.; Hummel, M.; Kahlenberg, V.; Wurst, K.; Nerdinger, S.; Schottenberger, H. Crystal Structure of 2-Ethylimidazole-1-Sulfonyl Azide: A New Azidation Reagent. Crystals 2012, 2, 118−126. (133) Goddard-Borger, E. D.; Stick, R. V. An Efficient, Inexpensive, and Shelf-Stable Diazotransfer Reagent: Imidazole-1-Sulfonyl Azide Hydrochloride. Org. Lett. 2007, 9, 3797−3800. (134) Fischer, N.; Goddard-Borger, E. D.; Greiner, R.; Klapötke, T. M.; Skelton, B. W.; Stierstorfer, J. Sensitivities of Some Imidazole-1Sulfonyl Azide Salts. J. Org. Chem. 2012, 77, 1760−1764. (135) Ye, H.; Liu, R.; Li, D.; Liu, Y.; Yuan, H.; Guo, W.; Zhou, L.; Cao, X.; Tian, H.; Shen, J.; Wang, P. G. A Safe and Facile Route to Imidazole-1-Sulfonyl Azide as a Diazotransfer Reagent. Org. Lett. 2013, 15, 18−21. (136) Van Dongen, S. F. M.; Teeuwen, R. L. M.; Nallani, M.; van Berkel, S. S.; Cornelissen, J. J. L. M.; Nolte, R. J. M.; van Hest, J. C. M. Single-Step Azide Introduction in Proteins via an Aqueous Diazo Transfer. Bioconjugate Chem. 2009, 20, 20−23. (137) Lartia, R.; Murat, P.; Dumy, P.; Defrancq, E. Versatile Introduction of Azido Moiety into Oligonucleotides through Diazo Transfer Reaction. Org. Lett. 2011, 13, 5672−5675. (138) Bastian, A. A.; Warszawik, E. M.; Panduru, P.; Arenz, C.; Herrmann, A. Regioselective Diazo-Transfer Reaction at the C3Position of the 2-Desoxystreptamine Ring of Neamine Antibiotics. Chem. - Eur. J. 2013, 19, 9151−9154. (139) Johansson, H.; Pedersen, D. S. Azide- and Alkyne-Derivatised A-Amino Acids. Eur. J. Org. Chem. 2012, 2012, 4267−4281. (140) Bowen, J. L.; Kelly, M. A.; Gumbleton, M.; Davies, P. R.; Allender, C. J. A Simple Zero Length Surface-Modification Approach for Preparing Novel Bifunctional Supports for Co-Immobilisation Studies. Tetrahedron Lett. 2012, 53, 3727−3730. (141) Lundquist, J. T.; Pelletier, J. C. Improved Solid-Phase Peptide Synthesis Method Utilizing Alpha-Azide-Protected Amino Acids. Org. Lett. 2001, 3, 781−783. (142) Rijkers, D. T. S.; van Vugt, H. H. R.; Jacobs, H. J. F.; Liskamp, R. M. J. A Convenient Synthesis of Azido Peptides by Post-Assembly Diazo Transfer on the Solid Phase Applicable to Large Peptides. Tetrahedron Lett. 2002, 43, 3657−3660. (143) Hansen, M. B.; van Gurp, T. H. M.; van Hest, J. C. M.; Löwik, D. W. P. M. Simple and Efficient Solid-Phase Preparation of AzidoPeptides. Org. Lett. 2012, 14, 2330−2333. (144) Vlieghe, P.; Lisowski, V.; Martinez, J.; Khrestchatisky, M. Synthetic Therapeutic Peptides: Science and Market. Drug Discovery Today 2010, 15, 40−56. (145) Rodionov, V. O.; Fokin, V. V.; Finn, M. G. Mechanism of the Ligand-Free CuI-Catalyzed Azide-Alkyne Cycloaddition Reaction. Angew. Chem., Int. Ed. 2005, 44, 2210−2215. (146) Proteau-Gagné, A.; Rochon, K.; Roy, M.; Albert, P.-J.; Guérin, B.; Gendron, L.; Dory, Y. L. Systematic Replacement of Amides by 1,4-disubstituted[1,2,3]triazoles in Leu-Enkephalin and the Impact on the Delta Opioid Receptor Activity. Bioorg. Med. Chem. Lett. 2013, 23, 5267−5269. 13


Review

ACS Combinatorial Science (147) Hausner, S. H.; Marik, J.; Gagnon, M. K. J.; Sutcliffe, J. L. In Vivo Positron Emission Tomography (PET) Imaging with an Alpha v Beta 6 Specific Peptide Radiolabeled Using 18F-“Click” Chemistry: Evaluation and Comparison with the Corresponding 4-[18F]fluorobenzoyl- and 2-[18F]fluoropropionyl-Peptides. J. Med. Chem. 2008, 51, 5901−5904. (148) Norgren, A.; Budke, C.; Majer, Z.; Heggemann, C.; Koop, T.; Sewald, N. On-Resin Click-Glycoconjugation of Peptoids. Synthesis 2009, 3, 488−494. (149) Rechenmacher, F.; Neubauer, S.; Mas-Moruno, C.; Dorfner, P. M.; Polleux, J.; Guasch, J.; Conings, B.; Boyen, H.-G.; Bochen, A.; Sobahi, T. R.; Burgkart, R.; Spatz, J. P.; Fässler, R.; Kessler, H. A Molecular Toolkit for the Functionalization of Titanium-Based Biomaterials That Selectively Control Integrin-Mediated Cell Adhesion. Chem. - Eur. J. 2013, 19, 9218−9223. (150) Liu, Y.; Zhang, L.; Wan, J.; Li, Y.; Xu, Y.; Pan, Y. Design and Synthesis of Cyclo[-Arg-Gly-Asp-Ψ(triazole)-Gly-Xaa-] Peptide Analogues by Click Chemistry. Tetrahedron 2008, 64, 10728−10734. (151) Schweinsberg, C.; Maes, V.; Brans, L.; Blauenstein, P.; Tourwe, D. A.; Schubiger, P. A.; Schibli, R.; Garayoa, E. G. Novel Glycated [99mTc(CO)3]-Labeled Bombesin Analogues for Improved Targeting of Gastrin-Releasing Peptide Receptor-Positive Tumors. Bioconjugate Chem. 2008, 19, 2432−2439. (152) Liu, T.; Qian, Z.; Xiao, Q.; Pei, D. High-Throughput Screening of One-Bead-One-Compound Libraries: Identification of Cyclic Peptidyl Inhibitors against calcineurin/NFAT Interaction. ACS Comb. Sci. 2011, 13, 537−546. (153) Lee, S. S.; Lim, J.; Cha, J. Peptide Libraries for Screening and Other Applications. Patent WO 2012/026887, 2012. (154) Aucagne, V.; Valverde, I. E.; Marceau, P.; Galibert, M.; Dendane, N.; Delmas, A. F. Towards the Simplification of Protein Synthesis: Iterative Solid-Supported Ligations with Concomitant Purifications. Angew. Chem., Int. Ed. 2012, 51, 11320−11324. (155) Hüttl, C.; Hettrich, C.; Riedel, M.; Henklein, P.; Rawel, H.; Bier, F. F. Development of Peptidyl Lysine Dendrons: 1,3-Dipolar Cycloaddition for Peptide Coupling and Antibody Recognition. Chem. Biol. Drug Des. 2015, 85, 565−573. (156) He, A.; Sheng, S.; Huang, Z.; Liu, L.; Cai, M. Solid-Phase Organic Synthesis of 1, 4- N -Vinyl- and 1, 4- N -Allyl-Triazoles with the Sulfonate Linker. J. Heterocycl. Chem. 2014, 51, 1862−1865. (157) Zabrodski, T.; Baskin, M.; Kaniraj, P.; Maayan, G. Click To Bind: Microwave-Assisted Solid-Phase Synthesis of Peptoids Incorporating Pyridine−Triazole Ligands and Their Copper(II) Complexes. Synlett 2015, 26, 461−466. (158) Holub, J. M.; Jang, H.; Kirshenbaum, K. Clickity-Click: Highly Functionalized Peptoid Oligomers Generated by Sequential Conjugation Reactions on Solid-Phase Support. Org. Biomol. Chem. 2006, 4, 1497−1502. (159) Gasser, G.; Hüsken, N.; Köster, S. D.; Metzler-Nolte, N. Synthesis of Organometallic PNA Oligomers by Click Chemistry. Chem. Commun. (Cambridge, U. K.) 2008, 3675−3677. (160) Qiu, J.; El-Sagheer, A. H.; Brown, T. Solid Phase Click Ligation for the Synthesis of Very Long Oligonucleotides. Chem. Commun. (Cambridge, U. K.) 2013, 49, 6959−6961. (161) Paritala, H.; Suzuki, Y.; Carroll, K. S. Efficient MicrowaveAssisted Solid Phase Coupling of Nucleosides, Small Library Generation and Mild Conditions for Release of Nucleoside Derivatives. Tetrahedron Lett. 2013, 54, 1869−1872. (162) Yamada, T.; Peng, C. G.; Matsuda, S.; Addepalli, H.; Jayaprakash, K. N.; Alam, M. R.; Mills, K.; Maier, M. A.; Charisse, K.; Sekine, M.; Manoharan, M.; Rajeev, K. G. Versatile Site-Specific Conjugation of Small Molecules to siRNA Using Click Chemistry. J. Org. Chem. 2011, 76, 1198−1211. (163) Meyer, A.; Vasseur, J.-J.; Morvan, F. Synthesis of Monoconjugated and Multiply Conjugated Oligonucleotides by “Click Thiol” Thiol-Michael-Type Additions and by Combination with CuAAC “Click Huisgen. Eur. J. Org. Chem. 2013, 2013, 465−473.

(164) Morvan, F.; Meyer, A.; Vasseur, J.-J.; Vidal, S.; Cloarec, J.; Chevolot, Y.; Souteyrand, E. Method for the Synthesis of Oligonucleotide Derivatives. Patent WO 2007/125429, 2007. (165) Crumpton, J. B.; Santos, W. L. Site-Specific Incorporation of Diamondoids on DNA Using Click Chemistry. Chem. Commun. (Cambridge, U. K.) 2012, 48, 2018−2020. (166) Loaiza, P. R.; Löber, S.; Hübner, H.; Gmeiner, P. Parallel Synthesis of Potent Dopaminergic N-Phenyltriazole Carboxamides Applying a Novel Click Chemistry Based Phenol Linker. Bioorg. Med. Chem. 2009, 17, 5482−5487. (167) Alexandra, L. F.; Vicent, L.; Celine, P.; Sami, B.; Kaynoush, N. Kit Useful for Detecting, Separating and/or Characterizating a Molecule of Interest. Patent WO 2010/029504, 2010. (168) Funder, E. D.; Jensen, A. B.; Tørring, T.; Kodal, A. L. B.; Azcargorta, A. R.; Gothelf, K. V. Synthesis of Dopamine and Serotonin Derivatives for Immobilization on a Solid Support. J. Org. Chem. 2012, 77, 3134−3142. (169) David, H.; Mantovani, G.; Ladmiral, V. Polymers. Patent WO 2007/104948, 2007. (170) Ortega-Muñoz, M.; Lopez-Jaramillo, J.; Hernandez-Mateo, F.; Santoyo-Gonzalez, F. Synthesis of Glyco-Silicas by Cu(I)-Catalyzed “Click-Chemistry” and Their Applications in Affinity Chromatography. Adv. Synth. Catal. 2006, 348, 2410−2420. (171) Li, X.; Shen, G.; Zhang, F.; Yang, B.; Liang, X. Click Aspartic Acid as H ILIC SPE Material for Selective Enrichment of N-Linked Glycopeptides. J. Chromatogr. B: Anal. Technol. Biomed. Life Sci. 2013, 941, 45−49. (172) Wang, Y.; Assaf, Z.; Liu, X.; Ziarelli, F.; Latifi, A.; Lamrabet, O.; Quéléver, G.; Qu, F.; Zhang, C.-C.; Peng, L. A “Click” Chemistry Constructed Affinity System for 2-Oxoglutaric Acid Receptors and Binding Proteins. Org. Biomol. Chem. 2014, 12, 6470−6475.

14


CuAAC: An Efficient Click Chemistry Reaction on ... - ACS Publications

Recommend Documents