TiO2 Photocatalysis in Aromatic âRedox Tagâ-Guided Intermolecular

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TiO2 Photocatalysis in Aromatic “Redox Tag”Guided Intermolecular Formal [2 + 2] Cycloadditions Yohei Okada, Naoya Maeta, Kaii Nakayama, and Hidehiro Kamiya J. Org. Chem., Just Accepted Manuscript • DOI: 10.1021/acs.joc.8b00738 • Publication Date (Web): 15 Apr 2018 Downloaded from http://pubs.acs.org on April 15, 2018

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The Journal of Organic Chemistry

TiO2 Photocatalysis in Aromatic “Redox Tag”Guided Intermolecular Formal [2 + 2] Cycloadditions Yohei Okada,* Naoya Maeta, Kaii Nakayama, Hidehiro Kamiya Department of Chemical Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588, Japan.

ABSTRACT

Since the pioneering work by Macmillan, Yoon, and Stephenson, homogeneous photoredox catalysis has occupied a central place in new reaction development in the field of organic chemistry. While heterogeneous semiconductor photocatalysis has also been studied extensively, it has generally been recognized as a redox option in inorganic chemistry where such “photocatalysis” is most often used to catalyze carbon-carbon bond cleavage, and not in organic chemistry where

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bond formation is usually the focal point. Herein, we demonstrate that titanium dioxide (TiO2) photocatalysis is a powerful redox option to construct carbon-carbon bonds by using intermolecular formal [2 + 2] cycloadditions as models. Synergy between excited electrons and holes generated upon irradiation is expected to promote the overall net redox neutral process. Key for the successful application is the use of a lithium perchlorate (LiClO4)/nitromethane (CH3NO2) electrolyte solution, which exhibits remarkable Lewis acidity to facilitate the reactions of carboncentered radical cations with carbon nucleophiles. The reaction mechanism is reasonably understood based on both intermolecular and intramolecular single electron transfer (SET) regulated by an aromatic “redox tag.” Most of the reactions were completed in less than 30 min even in aqueous and/or aerobic conditions without the need for sacrificial reducing or oxidizing substrates generally required for homogeneous photoredox catalysis.

INTRODUCTION Light has the potential to serve as a green and sustainable reagent to catalyze chemical reactions. Stemming from the pioneering work of Honda and Fujishima in 1972,1 titanium dioxide (TiO2) has occupied a central place in the field of semiconductor photocatalysis.2 The excited electron/hole pair generated upon irradiation in aqueous aerobic conditions produces reactive oxygen species (ROS)3 at the surface, which account for subsequent redox transformations. These species rapidly convert organic compounds into CO2 and H2O via carbon-carbon bond cleavage, therefore, semiconductor photocatalysis has generally been recognized as a redox option in inorganic chemistry but not in organic chemistry where carbon-carbon bond formation is the focal point. Nevertheless, the idea that the controlled application of semiconductor photocatalysis would


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be a green and sustainable synthetic procedure in organic chemistry has been proposed and it has been demonstrated to catalyze various redox transformations,4 typically radical-driven reactions involving a single electron transfer (SET) process.5 While semiconductor photocatalysis is a heterogeneous process, a homogeneous alternative is achieved by the use of transition metal complexes, which is now well-known as “photoredox catalysis.” The early work by MacMillan,6 Yoon,7 and Stephenson8 has triggered explosive growth in new reaction developments in this area.9 Arguably, heterogeneous semiconductor photocatalysis has taken a backseat to homogeneous photoredox catalysis in the field of organic chemistry. However, as clearly pointed out by Kisch,4(a) homogeneous photoredox catalysis generally requires the presence of sacrificial reducing or oxidizing substrates to quench either excited electrons or holes, otherwise recombination rapidly takes place. This differs from heterogeneous semiconductor photocatalysis, in that both reductive and oxidative SETs can potentially be enabled by excited electrons and holes, which might be advantageous over homogeneous photoredox catalysis. For TiO2 photocatalysis to be effective in carbon-carbon bond formation,10 the reactions must be carried out in dry anaerobic conditions in order not to produce ROS that can damage organic compounds. However, a striking testament to the utility of TiO2 photocatalysis in aerobic conditions has recently been proposed by Wang,11 where they described that challenging carboncarbon bond formation does occur if the reaction of the carbon-centered radical cation produced by hole oxidation with a carbon nucleophile is sufficiently more favorable than undesired oxygenation by ROS.


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We have been developing carbon-carbon bond formation reactions by electrocatalysis in lithium perchlorate (LiClO4)/nitromethane (CH3NO2) electrolyte solution.12 Our reaction design involves the aromatic “redox tag” concept,13 in which an aromatic ring provides both the oxidant and the reductant in the overall net redox neutral carbon-carbon bond formation reaction. In most cases, the use of LiClO4/CH3NO2 electrolyte solution is critical, because it exhibits remarkable Lewis acidity14 which facilitates the reactions of carbon-centered radical cations with carbon nucleophiles, even unactivated alkenes.15 Our reaction development is also characterized by the importance of an intramolecular SET process, which has recently been presented by Melchiorre as an elegant “electron relay” mechanism.16 We anticipated that the use of LiClO4/CH3NO2 electrolyte solution would pave the way for carbon-carbon bond formation by TiO2 photocatalysis. It should also be noted that overall net redox neutral processes would benefit from the involvement of both reductive and oxidative SETs potentially enabled by excited electrons and holes. Described herein is the aromatic redox tag-guided intermolecular formal [2 + 2] cycloaddition by TiO2 photocatalysis.

RESULTS AND DISCUSSION The present work began with the reaction between the enol ether (1) and 1-hexene (2) as a model17, 18

using Aeroxide P25, which is considered to be the “gold standard” for TiO2 photoctalysis (Table

1). The catalyst consists of roughly 75% anatase and 25% rutile, which exhibit a synergistic effect, and is much more active than anatase or rutile alone.19 Based on the characterization by Brunauer– Emmett–Teller (BET) theory using adsorption isotherms of nitrogen, the specific surface area was estimated to be 52.3 m2/g.


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Table 1. Optimization of the Conditions for the [2 + 2] Cycloaddition.

The results were much better than expected: the reaction was complete in 3 min to give the desired cycloadduct (3) (entries 1-3). When the reaction was stopped at 1 min, the yield significantly dropped off, even though the enol ether (1) was almost completely consumed, suggesting that the rate-limiting step is nucleophilic attack rather than hole oxidation (entry 4). No desired cycloadduct (3) was obtained in the absence of TiO2 under the dark condition (entry 5) and enol


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ether (1) was recovered. This was not the case for the reaction carried out in the presence of TiO2 under the dark condition (entry 6), which resulted in inseparable aldehyde mixtures, probably due to acidic hydrolysis of the enol ether (1). When the reaction was carried out in the absence of TiO2 under irradiation, a trace amount of the cycloadduct (3) was obtained (entry 7). Surprisingly, the reaction took place smoothly even in aqueous and/or aerobic conditions (entries 8-10), showing that the reaction of the radical cation (1.+) produced by hole oxidation with 1-hexene (2) is more favorable than undesired oxygenation by ROS. It should be noted that no oxygenated products were observed under our reaction conditions. While it is not clear if the reaction is “parallel” and/or “anti-parallel,” significant dimerization of the enol ether (1) occurred in the reaction. The dimer (4) is expected to form via the reaction of the radical cation (1.+) produced by hole oxidation with the neutral enol ether (1), even in the presence of 20 eq (1.0 M) of 1-hexene (2). Although it is likely that the neutral enol ether (1) has higher nucleophilicity than 1-hexene (2) due to its electron density, even so, these observations seem to be beyond the range of statistical probability. It could be postulated that enol ether (1) was anchored onto the TiO2 surface, creating a local high concentration, which resulted in dimerization. If this hypothesis is correct, it is not the large excess of 1-hexene (2) but the loading amount of the enol ether (1) per unit area of the TiO2 surface that would be the key to suppressing the dimerization. Therefore, the selectivity of cycloadduct (3)/dimer (4) was investigated under modified conditions (Table 2). To our delight, the yield of cycloadduct (3) finally reached 87% yield with a decreased amount of the dimer (4), when 4 mol/m2 of the enol ether (1) for the TiO2 surface was used (Table 2, entry 5).


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Table 2. Competition Experiments between the [2 + 2] Cycloaddition and Dimerization.

This hypothesis was unambiguously confirmed by control experiments using 1-decene (5), enol ether (6) and alkene (7) (Scheme 1). The reaction between enol ether (1) and 1-decene (5) gave the desired cycloadduct (8) in good yield by either electrocatalysis or photocatalysis. On the other hand, based on the oxidation potentials (Figures S3 and S4), the selective oxidation of the enol ether (6) would be possible even in the presence of the alkene (7), and indeed the reaction gave the desired cycloadduct (8) by electrocatalysis, whereas only a trace amount of the cycloadduct (8) was obtained under optimized photocatalysis conditions. Thus it can be concluded that the hole


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oxidation in TiO2 photocatalysis is guided by the aromatic ring, enabling unique selectivity beyond the oxidation potentials (Figure 1). Presumably, the reaction began with the fast anchoring of the enol ether (1) onto the TiO2 surface, followed by rapid hole oxidation to produce the radical cation (1.+), which was then trapped by 1-hexene (2) in the rate limiting step to generate transient cyclobutyl radical cation (3c.+). The aromatic ring then functioned as a redox tag to reduce the cyclobutyl radical cation to give relatively long-lived aromatic radical cation (3a.+). Since the excited electron was able to reduce the thus formed aromatic radical cation (3a.+) simultaneously, the overall processes were completed to give the desired cycloadduct (3) in a couple of minutes.

Scheme 1. Control Experiments for the [2 + 2] Cycloaddition.

Figure 1. Plausible Reaction Mechanism for the [2 + 2] Cycloaddition.


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With the optimized conditions in hand, the reactions of enol ether (1) with several hexenes (9–14) were conducted to test the functional group tolerance (Table 3). It should be noted that a pendant oxygen atom was found to be compatible with the reaction, even without an electron-withdrawing substituent, since ether (11) and alcohol (12) afforded the desired cycloadducts (17, 18) in good yields, respectively. These observations are in marked contrast to the previous reports, where a competitive donation of the oxygen electron(s) into the radical cation seems to occur.20 This might stem from the use of the LiClO4/CH3NO2 electrolyte solution, which facilitates the nucleophilic attack of unactivated alkenes to carbon-centered radical cations. On the other hand, the carboxylic acid (13) gave no desired cycloadduct (19), while the desired cycloadduct (20) was obtained in good yield from the ester (14). Since a carboxylic acid is a potential anchoring group for the TiO2 surface,21 competitive anchoring of the carboxylic acid (13) onto the TiO2 surface would take place, which inhibits hole oxidation of the enol ether (1). Although this is indeed a negative effect for the reaction, the surface could also be positively modified with designed ligands as recently pointed out by Weiss,22 which would be a unique advantage for heterogeneous semiconductor photocatalysis over homogeneous photoredox catalysis.


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Table 3. Hexene Variation for the [2 + 2] Cycloaddition.a ,b

To understand the distinctive reactivity unique to the radical cation (1.+), several alkenes (21–25) were also tested instead of 1-hexene (2) (Table 4). 1,1-Disubstituted alkene (21) was found to be comparable to 1-hexene (2), while 1,2-disubstituted alkenes (22, 23) were significantly less effective, affording inseparable diastereomixtures (27). Although tetrasubstituted alkene (25) was also less effective for the reaction, trisubstituted alkene (24) was unexpectedly found to be comparable to terminal alkenes (2, 21). This could be explained as a result of the trade-off between


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kinetic and thermodynamic reactivity of the radical cation (1.+), which would be a complementary intermediate to the radical and/or cation.

Table 4. Alkene Variation for the [2 + 2] Cycloaddition.a ,b

The scope of the aromatic redox tag in the [2 + 2] cycloaddition was investigated next using enol ethers with variously substituted aromatic rings (30–44) (Table 5). In accordance with our previous observations, non-substituted phenyl ring (45) was not effective for the reaction, which is


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presumably due to ineffective intramolecular SET to reduce the transient cyclobutyl radical cation (Scheme 2, SET B). In addition to phenoxy (46) and siloxy (47) groups, a free hydroxy group (48) was proven to be a productive substituent. The decreased yield is probably due to the acidic proton, which potentially induces proton-coupled electron transfer under the photocatalysis conditions that alters the reaction mode. The positioning of the methoxy group was found to be critical, as the ortho-substitution (49) was comparably effective to the para-variant (1), while meta-substitution (50) was less effective. Installation of additional methoxy groups was also found to be disadvantageous for the reaction (51–54), which can be formally understood by an equilibrium illustrated via an intramolecular SET (Scheme 2, SET A). The radical and/or cation was potentially localized on either the enol ether moiety or aromatic ring. For effective trapping by 1-hexene (2) to form the cyclobutyl radical cation, significant reactivity must exist on the enol ether moiety rather than on the aromatic ring. When additional methoxy groups are installed, the respective aromatic radical cations are expected to be highly stabilized. In other words, the radical and/or cation would mainly be localized on the aromatic ring, thus rendering it unable to participate in further bond formation. On the other hand, weakly electron-donating methyl groups were proven to be an effective tuning motif for the aromatic redox tag, namely, the yields of the respective cycloadducts (55–57) were reasonably increased in relation to the number of methyl groups. The sulfide (58) was also found to be a promising substrate, while the amine (59) was not. These observations suggest that basicity is also critical for the reaction, since the LiClO4/CH3NO2 electrolyte solution exhibits Lewis acidity.

Table 5. Aromatic Redox Tag Variation for the [2 + 2] Cycloaddition.a ,b


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Scheme 2. Plausible Reaction Mechanism for the [2 + 2] Cycloaddition.

Further mechanistic studies were attempted to illustrate the overall picture of the reaction by using cyclic voltammetry (CV) measurements in conjunction with density functional theory (DFT) calculations carried out at the B3LYP/6-311G++(2d,2p) level. The shapes of orbitals and spin densities would be helpful to determine which portions of the substrates were engaged in SET processes in the reactions. The standard para-methoxy enol ether (1) showed an oxidation peak at


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1.36 V vs. Ag/AgCl with a negligible reduction wave (Figure 2). The orbital plot for the optimized structure showed that the HOMO, where oxidative SET is expected to occur, was localized on both the enol ether moiety and aromatic ring and indeed, spin density was distributed along the HOMO in its radical cation form (1.+). Similar results were obtained for the ortho-methoxy enol ether (34) with an oxidation peak at 1.39 V vs. Ag/AgCl accompanied by a slight reduction wave, suggesting some reversibility (Figure 3). In contrast, the less effective meta-methoxy enol ether (35) exhibited a totally different oxidation wave of several peaks, with the lowest one recorded at 0.87 V vs. Ag/AgCl (Figure 4). The HOMO was dominantly found on the enol ether moiety, where spin density was overlapping. It should be noted that the ineffective non-substituted enol ether (30) also possessed a similar HOMO and spin density with an oxidation peak at 1.25 V vs. Ag/AgCl (Figure 5). In light of the fact that para- and ortho-methoxy enol ethers (1, 34) showed oxidation peaks at 1.36 and 1.39 V vs. Ag/AgCl, respectively, the values measured for meta-methoxy enol ether (35) and non-substituted enol ether (30) were unexpectedly low and cannot simply be understood based on their molecular structures. These results seem to suggest that the enol ether moieties and aromatic rings were electronically separated in the cases of non-substituted and meta-methoxy enol ethers (30, 35), even though they were tethered together by ethylene linkers, which might render these substrates less or ineffective for the reactions. However, both CVs and spin densities indicated that oxidative SET should be possible even for these unsuccessful enol ethers (30, 35) and the generated radical cations were expected to have significant reactivity at their enol ether moieties. Therefore, it is assumed that trapping by 1-hexene (1) would also be possible and the respective intramolecular SET (SET B in Scheme 2) might be the key to understanding the unsuccessful reactions. On the other hand, the disadvantageous effect caused by the installation of additional methoxy groups was supported by both CV measurements and DFT calculations,


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namely, significantly lower oxidation peaks were measured for both 2,4-dimethoxy- and 2,4,6trimethoxy enol ethers (36, 37) (Figures 6 and 7). In these cases, two distinct oxidation peaks were observed, which could be assigned to the aromatic rings and enol ether moieties, suggesting that they were also electronically separated from each other. It is perhaps fair to say that electron densities of the aromatic rings and enol ether moieties must be balanced for the electronic interactions to occur, which is crucial for the successful reactions. Additionally, spin densities of 2,4-dimethoxy- and 2,4,6-trimethoxy enol ethers (36, 37) were mainly distributed on the aromatic rings, suggesting that the formal understanding of SET A in Scheme 2 is reasonable.

Figure 2. CV Measurements and DFT Calculations of para-Methoxy Enol Ether (1).

Figure 3. CV Measurements and DFT Calculations of ortho-Methoxy Enol Ether (34).


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Figure 4. CV Measurements and DFT Calculations of meta-Methoxy Enol Ether (35).


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Figure 5. CV Measurements and DFT Calculations of Non-Substituted Enol Ether (30).

Scheme 3. Spin Densities and HOMOs of Plausible Reaction Mechanism for the [2 + 2] Cycloaddition. Calculations were carried out with a methyl group instead of the n-butyl group for simplification.


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Figure 6. CV Measurements and DFT Calculations of 2,4-Dimethoxy Enol Ether (36).


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Figure 7. CV Measurements and DFT Calculations of 2,4,6-Trimethoxy Enol Ether (37).

To gain mechanistic insights into SET B in Scheme 2, DFT calculations were performed using the cycloadducts (3, 45) as typical successful and unsuccessful models. In good accordance with our formal expression of the reaction mechanism, the spin density was selectively found in the aromatic rings in the optimized structures of the radical cation (3.+), which seems to be the aromatic radical cation (3a.+) rather than the cyclobutyl radical cation (3c.+). The orbital plot for the optimized structure of the neutral cycloadduct (3) showed that the HOMO nicely overlapped the spin density of its radical cation (3.+). The oxidative SET for the neutral cycloadduct (3) is expected to take place from the HOMO, where the reductive SET to the radical cation (3.+) should also be involved. On the basis of this hypothesis, both the spin density and HOMO nicely illustrate our formal mechanistic understanding. However, in the optimized structures of the radical cation (45.+), the spin density remained in the cyclobutyl moieties, i.e., the cyclobutyl radical cation (45c.+) rather


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than the aromatic radical cation (45a.+). Furthermore, one carbon-carbon bond that constructs the cyclobutyl framework was found to be elongated, indicating incomplete ring formation, which also supports our formal expression of the reaction mechanism. On the other hand, the HOMO was mainly distributed on the aromatic ring in the optimized structure of the neutral cycloadduct (45), where no elongated carbon-carbon bond was observed in the cyclobutyl framework. Therefore, reductive SET to the radical cation (45.+) is expected to take place on the aromatic ring, if the intramolecular SET (SET B in Scheme 2) is possible. Taken together, the overall picture of the reaction mechanism is rationally illustrated on the basis of dual intramolecular SET processes (SET A and SET B in Scheme 2), which were regulated by the aromatic redox tag.

CONCLUSION In conclusion, we have demonstrated that TiO2 photocatalysis is a powerful redox option to construct carbon-carbon bonds by using intermolecular formal [2 + 2] cycloadditions as models. Most of the reactions were completed in less than 30 min even in aqueous and/or aerobic conditions, which was probably attributed to the synergy between the excited electron and hole generated upon irradiation that promoted the overall net redox neutral process. It should be noted that sacrificial reducing or oxidizing substrates generally required for homogeneous photoredox catalysis were not needed for these reactions. The use of LiClO4/CH3NO2 electrolyte solution was also key for the successful applications, since it exhibited a remarkable Lewis acidity that facilitated the reactions of carbon-centered radical cations with carbon nucleophiles. The overall picture of the reaction mechanism was illustrated on the basis of both intermolecular and intramolecular SET processes regulated by an aromatic redox tag, which was reasonably supported by CV


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measurements and DFT calculations. We believe that the results described herein will enhance the application of heterogeneous semiconductor photocatalysis in the field of synthetic organic chemistry. Further design and development of reactions guided by this redox tag concept in combination with semiconductor photocatalysis is under investigation in our laboratory.

EXPERIMENTAL SECTION General Remarks: All reagents and solvents were purchased from commercial sources and used without further purification. Reactions were monitored by thin-layer chromatography (TLC) carried out on silica gel plates, with detection by UV absorption (254 nm) and by heating the plates after dipping them in a solution of 12 M molybdo(VI) phosphoric acid n-hydrate in 95% ethanol. Silica gel (particle size 40−50 μm) was used for column chromatography. 1H NMR spectra were collected on a 500 MHz NMR spectrometer using the deuterated solvent as an internal deuterium reference. Chemical shift data are given in δ units calibrated with residual protic solvent. The multiplicity of a signal is indicated as follows: s, singlet; d, doublet; t, triplet; q, quartet; quint, quintet; m, multiplet. 13C{1H} NMR spectra were collected at 125 MHz with proton decoupling using the deuterated solvent as an internal carbon reference. Chemical shift data are given in δ units calibrated with residual solvent. High-resolution mass spectra (HRMS) were collected on electrospray ionization (ESI)- or direct analysis in real time (DART)-time-of-flight (TOF) spectrometers.

Synthesis and Characterization Data.


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General Procedure for the Synthesis of Enol Ethers (from Substituted Phenylpropionic Acids): The enol ethers were synthesized from the respective substituted phenylpropionic acids (if available) in 3 steps, including Weinreb amide synthesis, lithium aluminum hydride reduction, and Wittig reaction. To a solution of the respective substituted phenylpropionic acid (30.0 mmol) and N,O-dimethylhydroxylamine hydrochloride (4.39 g, 45.0 mmol) in dichloromethane (80 mL) stirred at room temperature were added N,N'-diisopropylcarbodiimide (6.97 mL, 45.0 mmol), 4dimethylaminopyridine (36.7 ng, 0.30 mmol), and N,N-diisopropylethylamine (10.3 mL, 60.0 mmol). The resulting reaction mixture was stirred at room temperature overnight, diluted with water, and extracted with dichloromethane. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (hexane/ethyl acetate = 1/1) gave the respective Weinreb amides in 61−67% yield. To a solution of the respective Weinreb amide (18.0 mmol) in tetrahydrofuran (80 mL) stirred at 0 °C was added lithium aluminum hydride (751 mg, 19.8 mmol). The resulting reaction mixture was stirred at 0 °C until the starting material was consumed (checked by thin layer chromatography), diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, concentrated in vacuo, and used without further purification. To a solution of (methoxymethyl)triphenylphosphonium chloride (12.3 g, 36.0 mmol) in tetrahydrofuran (80 mL) stirred at 0 °C was added potassium tert-butoxide (3.03 g, 27.0 mmol). After the color turned red, the crude aldehyde was added, stirred at 0 °C until the starting material was consumed (checked by thin layer chromatography), diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (hexane/ethyl acetate = 20/1) gave the desired enol ethers in 28−31% yield over 2 steps.


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General Procedure for the Synthesis of Enol Ethers (from the Respective Substituted Benzaldehydes): The enol ethers were synthesized from the respective substituted benzaldehydes (if the corresponding substituted phenylpropionic acids were not available) in 5 steps including Wittig reaction and acid hydrolysis. To a solution of (methoxymethyl)triphenylphosphonium chloride (34.3 g, 100.0 mmol) in tetrahydrofuran (160 mL) stirred at 0 °C was added potassium tert-butoxide (8.42 g, 75.0 mmol). After the color turned red, the respective substituted benzaldehyde (50.0 mmol) was added, and the reaction was stirred at 0 °C until the starting material was consumed (checked by thin layer chromatography), diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (hexane/ethyl acetate = 20/1) gave the respective enol ethers in 87−93% yield. To a solution of the respective enol ether (45.0 mmol) in acetone (100 mL) stirred at room temperature was added a catalytic amount of concentrated sulfuric acid. The resulting reaction mixture was stirred at room temperature until the starting material was consumed (checked by thin layer chromatography), diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (hexane/ethyl acetate = 5/1) gave the respective substituted benzaldehydes in 35−40% yield. The repetitive Wittig reactions and acid hydrolysis gave the desired enol ethers in 25−30% yield over 3 steps.

General Procedure for the [2 + 2] Cycloadditions: To a solution of LiClO4 (1.0 M) in CH3NO2 stirred at room temperature were added the respective enol ethers and alkenes. The resulting


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reaction mixture was stirred at room temperature in front of a 15 W UV lamp (350 nm) until the starting material was consumed (checked by thin layer chromatography), diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Yields were determined by 1H NMR analysis using benzaldehyde as an internal standard. Silica gel column chromatography (hexane/ethyl acetate = 50/1) gave the desired cycloadduct.

1-Methoxy-4-(4-methoxybut-3-en-1-yl)benzene (1, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.12 (2H, d, J = 8.6 Hz), 6.82 (2H, d, J = 8.6 Hz), 5.87 (1H, dt, J = 6.3, 1.7 Hz), 4.36 (1H, dt, J = 7.3, 6.3 Hz), 3.78 (3H, s), 3.56 (3H, s), 2.60 (2H, t, J = 7.3 Hz), 2.35 (2H, dq, J = 7.3, 1.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 146.5, 134.4, 129.4, 113.7, 106.1, 59.6, 55.3, 35.1, 25.9. trans: 1H NMR (CDCl3, 500 MHz)  7.09 (2H, d, J = 8.6 Hz), 6.83 (2H, d, J = 8.6 Hz), 6.29 (1H, dt, J = 12.6, 1.2 Hz), 4.74 (1H, dt, J = 12.6, 7.3 Hz), 3.79 (3H, s), 3.49 (3H, s), 2.59 (2H, t, J = 7.3 Hz), 2.20 (2H, dq, J = 7.3, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 147.5, 134.2, 129.5, 113.8, 102.3, 55.9, 55.3, 36.6, 30.1; HRMS [M + H]+ calculated for C12H17O2 193.1229, found 193.1250.


24

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1-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)-4-methoxybenzene (3, all trans). Colorless oil.

1

H NMR (CDCl3, 500 MHz)  7.08 (2H, d, J = 8.6 Hz), 6.81 (2H, d, J = 8.6 Hz), 3.78 (3H, s), 3.30

(3H, s), 3.11 (1H, t, J = 6.8 Hz), 2.59-2.43 (2H, m), 2.07-1.82 (4H, m), 1.65-1.53 (2H, m), 1.361.17 (5H, m), 0.88 (3H, t, J = 7.1 Hz), 0.72 (1H, q, J = 9.1 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 134.8, 129.4, 113.9, 86.6, 56.6, 55.4, 40.7, 40.2, 37.6, 35.1, 33.0, 29.8, 25.6, 22.9, 14.3; HRMS [M + H]+ calculated for C18H29O2 277.2168, found 277.2177.

4,4'-((3,4-Dimethoxycyclobutane-1,2-diyl)bis(ethane-2,1-diyl))bis(methoxybenzene)

(4).

Colorless oil.

1


(6H, s), 3.31-3.26 (2H, m), 2.62-2.45 (4H, m), 1.84-1.78 (4H, m), 1.48-1.43 (2H, m);

13

C{1H}

NMR (125 MHz, CDCl3)  157.9, 134.4, 129.3, 113.9, 85.0, 57.0, 55.4, 40.3, 37.1, 33.1; HRMS [M + H]+ calculated for C24H33O4 385.2380, found 385.2352.


25


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1-Methoxydec-1-ene (6, cis : trans = 1 : 2). Colorless oil.

To a solution of (methoxymethyl)triphenylphosphonium chloride (3.43 g, 10.0 mmol) in tetrahydrofuran (40 mL) stirred at 0 °C was added potassium tert-butoxide (842 g, 7.50 mmol). After the color turned red, nonanal (868 L, 5.00 mmol) was added, and the reaction was stirred at 0 °C until the starting material was consumed (checked by thin layer chromatography), diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (hexane) gave the enol ether (6) in 74% yield (630 mg, 3.70 mmol). cis: 1H NMR (CDCl3, 500 MHz)  5.86 (1H, dt, J = 6.3, 1.7 Hz), 4.34 (1H, dt, J = 7.5, 1.2 Hz), 3.58 (3H, s), 2.05 (2H, dq, J = 6.9, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  146.0, 107.3, 59.6, 31.0, 30.0, 29.7, 29.5, 29.2, 27.9, 24.1, 14.3. trans: 1H NMR (CDCl3, 500 MHz)  6.28 (1H, dt, J = 12.6, 1.2 Hz), 4.73 (1H, dt, J = 12.6, 6.9 Hz), 3.50 (3H, s), 1.91 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  147.0, 103.3, 56.0, 32.1, 30.0, 29.7, 29.5, 29.2, 27.9, 22.9, 14.3; HRMS [M + H]+ calculated for C11H23O 171.1750, found 171.1723.

1-(But-3-en-1-yl)-4-methoxybenzene (7). Colorless oil.


26

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To a solution of 4-methoxybenzyl chloride (2.72 mL, 20.0 mmol) in tetrahydrofuran (60 mL) stirred at 0 oC was added allylmagnesium bromide (0.7 mol/L in diethyl ether, 57.2 mL, 40.0 mmol). The resulting reaction mixture was stirred at 0 oC to room temperature overnight, diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (hexane/ethyl acetate = 30/1) gave the alkene (7) in 62% yield (2.01 g, 12.4 mmol). 1

H NMR (CDCl3, 500 MHz)  7.10 (2H, d, J = 8.6 Hz), 6.83 (2H, d, J = 8.6 Hz), 5.85 (1H, ddt, J

= 16.6, 10.3, 6.9 Hz), 5.03 (1H, dq, J = 16.6, 1.7 Hz), 4.97 (1H, dd, J = 10.9, 1.7 Hz), 3.79 (3H, s), 2.65 (2H, t, J = 7.5 Hz), 2.34 (2H, dt, J = 8.0, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3) d 157.9, 138.2, 133.9, 129.3, 114.9, 113.7, 55.1, 35.9, 34.5; HRMS [M + H]+ calculated for C11H15O 163.1124, found 163.1147.

1-Methoxy-4-(2-(2-methoxy-3-octylcyclobutyl)ethyl)benzene (8, alll trans). Colorless oil.

1


(3H, s), 3.10 (1H, t, J = 6.9 Hz), 2.57-2.44 (2H, m), 2.06-1.83 (4H, m), 1.65-1.52 (2H, m), 1.40-


27


Page 28 of 59

1.17 (13H, m), 0.88 (3H, t, J = 6.3 Hz), 0.71 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 134.8, 129.3, 113.8, 86.6, 56.6, 55.4, 40.7, 40.2, 37.6, 35.5, 32.9, 32.1, 29.9, 29.8, 29.5, 27.5, 25.6, 22.9, 14.3; HRMS [M + H]+ calculated for C22H37O2 333.2794, found 333.2813.

Hex-5-en-1-yl benzoate (9). Colorless oil.

To a solution of 5-hexen-1-ol (1.18 mL, 10.0 mmol) and trimethylamine (2.77 mL, 20.0 mmol) in tetrahydrofuran (30 mL) stirred at room temperature was added benzoyl chloride (1.74 mL, 15.0 mmol). The resulting reaction mixture was stirred at room temperature overnight, diluted with water, and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (hexane/ethyl acetate = 10/1) gave the hexene (9) in 93% yield (1.90 g, 9.30 mmol). 1

H NMR (CDCl3, 500 MHz)  8.04 (2H, d, J = 8.5 Hz), 7.55 (1H, t, J = 7.0 Hz), 7.44 (2H, t, J =

8.0 Hz), 5.82 (1H, ddt, J = 17.2, 10.3, 6.9 Hz), 5.03 (1H, dq, J = 17.2, 1.7 Hz), 4.97 (1H, dd, J = 10.3, 1.7 Hz), 4.33 (2H, t, J = 6.5 Hz), 2.13 (2H, dt, J = 7.5, 6.9 Hz), 1.79 (2H, quin, J = 7.5 Hz), 1.55 (2H, quin, J = 7.0 Hz); 13C{1H} NMR (125 MHz, CDCl3)  166.7, 138.4, 132.9, 130.5, 129.6, 128.4,; HRMS [M + H]+ calculated for C13H17O2 205.1229, found 205.1205.


28

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6-Methoxyhex-1-ene (11). Colorless oil.

To a solution of 5-hexen-1-ol (3.54 mL, 30.0 mmol) in diethyl ether (80 mL) stirred at room temperature was added sodium hydride (60%, dispersion in paraffin liquid, 1.44 g, 36.0 mmol). After stirring at room temperature for 30 min, methyl iodide (3.74 mL, 60.0 mmol) was added. The resulting reaction mixture was stirred at room temperature for overnight, diluted with water, and extracted with pentane. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Silica gel column chromatography (pentane) gave the hexene (11) in 42% yield (1.44 g, 12.6 mmol). 1

H NMR (CDCl3, 500 MHz) δ 5.81 (1H, ddt, J = 17.2, 10.3, 6.3 Hz), 5.01 (1H, dq, J = 17.2, 1.7

Hz), 4.95 (1H, d, J = 10.3 Hz), 3.38 (2H, t, J = 6.3 Hz), 3.33 (3H, s), 2.07 (2H, dt, J = 7.5, 6.9 Hz), 1.59 (2H, quin, J = 7.5 Hz), 1.45 (2H, quin, J = 7.5 Hz); 13C{1H} NMR (125 MHz, CDCl3) δ 138.8, 114.6, 72.8, 58.6, 33.7, 29.2, 25.6; HRMS [M + H]+ calculated for C7H15O 115.1124, found 115.1100.

4-(2-Methoxy-3-(4-methoxyphenethyl)cyclobutyl)butyl benzoate (15, all trans). Colorless oil.


29


1

Page 30 of 59

H NMR (CDCl3, 500 MHz) δ 8.04 (2H, dd, J = 8.6, 1.2 Hz), 7.55 (1H, tt, J = 6.6, 1.7 Hz), 7.44

(2H, t, J = 8.0 Hz), 7.08 (2H, d, J = 8.6 Hz), 6.81 (2H, d, J = 8.6 Hz), 4.31 (2H, t, J = 6.9 Hz), 3.78 (3H, s), 3.29 (3H, s), 3.12 (1H, t, J = 6.9 Hz), 2.57-2.45 (2H, m), 2.08-1.94 (3H, m), 1.92-1.85 (1H, m), 1.79-1.72 (2H, m), 1.69-1.58 (2H, m), 1.46-1.37 (3H, m), 0.74 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3) δ 166.8, 157.8, 134.7, 133.0, 130.6, 129.7, 129.3, 128.5, 113.9, 86.5, 65.7, 56.7, 55.4, 40.6, 40.3, 37.6, 35.0, 32.9, 28.9, 25.5, 24.0; HRMS [M + H]+ calculated for C25H33O4 397.2380, found 397.2392.

4-(2-Methoxy-3-(4-methoxyphenethyl)cyclobutyl)butyl acetate (16, all trans). Colorless oil.

1

H NMR (CDCl3, 500 MHz) δ 7.08 (2H, d, J = 8.6 Hz), 6.82 (2H, d, J = 8.6 Hz), 4.05 (2H, t, J =

6.9 Hz), 3.78 (3H, s), 3.29 (3H, s), 3.11 (1H, t, J = 6.9 Hz), 2.57-2.45 (2H, m), 2.05 (3H, s), 2.041.84 (3H, m), 1.65-1.57 (5H, m), 1.40-1.25 (3H, m), 0.72 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3) δ 171.4, 157.8, 134.6, 129.3, 113.9, 86.5, 64.7, 56.6, 55.4, 40.5, 40.3, 37.6, 34.9, 32.9, 28.8, 25.5, 23.9, 21.2; HRMS [M + H]+ calculated for C20H31O4 335.2223, found 335.2225.

1-Methoxy-4-(2-(2-methoxy-3-(4-methoxybutyl)cyclobutyl)ethyl)benzene (17, all trans). Colorless oil.


30

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1

H NMR (CDCl3, 500 MHz) δ 7.08 (2H, d, J = 8.6 Hz), 6.82 (2H, d, J = 8.6 Hz), 3.78 (3H, s), 3.36

(2H, t, J = 6.9 Hz), 3.32 (3H, s), 3.29 (3H, s), 3.11 (1H, t, J = 6.9 Hz), 2.56-2.45 (2H, m), 2.271.92 (2H, m), 1.91-1.83 (1H, m), 1.64-1.51 (5H, m), 1.38-1.25 (3H, m), 0.72 (1H, q, J = 9.7 Hz); C{1H} NMR (125 MHz, CDCl3) δ 157.8, 134.7, 129.4, 113.8, 86.5, 73.0, 58.7, 56.6, 55.4, 40.7,

13

40.2, 37.6, 35.3, 32.9, 29.9, 25.5, 24.2; HRMS [M + H]+ calculated for C19H31O3 307.2274, found 307.2281.

4-(2-Methoxy-3-(4-methoxyphenethyl)cyclobutyl)butan-1-ol (18, all trans). Colorless oil.

1


(2H, t, J = 6.3 Hz), 3.30 (3H, s), 3.12 (1H, t, J = 6.9 Hz), 2.57-2.45 (2H, m), 2.07-1.93 (2H, m), 1.92-1.84 (1H, m), 1.64-1.51 (4H, m), 1.41-1.26 (4H, m), 0.73 (1H, q, J = 9.2 Hz); 13C{1H} NMR (125 MHz, CDCl3) δ 157.8, 134.7, 129.4, 113.9, 86.5, 63.1, 56.6, 55.4, 40.6, 40.2, 37.6, 35.1, 32.9, 32.9, 25.6, 23.7; HRMS [M + H]+ calculated for C18H29O3 293.2117, found 293.2114.


31


Page 32 of 59

Methyl 4-(2-methoxy-3-(4-methoxyphenethyl)cyclobutyl)butanoate (20, all trans). Colorless oil.

1


(3H, s), 3.29 (3H, s), 3.11 (1H, t, J = 6.9 Hz), 2.54-2.44 (2H, m), 2.30 (2H, t, J = 5.7 Hz), 2.071.92 (3H, m), 1.91-1.84 (1H, m), 1.63-1.55 (4H, m), 1.40-1.33 (1H, m), 0.73 (1H, q, J = 9.7 Hz); C{1H} NMR (125 MHz, CDCl3) δ 174.3, 157.8, 134.6, 129.3, 113.8, 86.3, 56.6, 55.4, 51.6, 40.3,

13

40.2, 37.5, 34.7, 34.1, 32.8, 25.4, 22.9; HRMS [M + H]+ calculated for C19H29O4 321.2144, found 321.2165.

1-(2-(3,3-Diethyl-2-methoxycyclobutyl)ethyl)-4-methoxybenzene (26, trans). Colorless oil.

1


(3H, s), 3.15 (1H, d, J = 7.5 Hz), 2.57-2.44 (2H, m), 2.15-2.06 (1H, m), 1.91-1.83 (1H, m), 1.71 (1H, t, J = 10.3 Hz), 1.64-1.52 (3H, m), 1.50-1.41 (2H, m), 1.40-1.32 (1H, m), 0.82 (3H, t, J = 7.5 Hz), 0.81 (3H, t, J = 7.5 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 134.9, 129.4, 113.9, 88.1,


32

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58.1, 55.4, 45.1, 38.4, 38.1, 33.0, 31.4, 30.3, 23.3, 8.8, 8.1; HRMS [M + H]+ calculated for C18H29O2 277.2168, found 277.2181.

1-(2-(2,3-Diethyl-4-methoxycyclobutyl)ethyl)-4-methoxybenzene (27). Colorless oil.

1


(3H, s), 3.04 (1H, t, J = 6.9 Hz), 2.57 (2H, t, J = 8.0 Hz), 1.78-1.71 (2H, m), 1.71-1.65 (1H, m), 1.62-1.55 (1H, m), 1.54-1.46 (4H, m), 1.09-1.02 (1H, quin, J = 7.5 Hz), 0.91 (3H, t, J = 7.5 Hz), 0.87 (3H, t, J = 7.5 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 135.0, 129.3, 113.9, 84.0, 56.5, 55.4, 48.1, 46.0, 40.7, 37.6, 33.2, 29.1, 27.8, 12.1; HRMS [M + H]+ calculated for C18H29O2 277.2168, found 277.2168.

1-(2-(2-Ethyl-4-methoxy-3,3-dimethylcyclobutyl)ethyl)-4-methoxybenzene

(28,

all

trans).

Colorless oil.


33


1

Page 34 of 59


(3H, s), 2.98 (1H, d, J = 7.5 Hz), 2.58-2.49 (2H, m), 1.79-1.67 (3H, m), 1.37 (2H, dq, J = 8.0, 7.5 Hz), 1.16 (3H, s), 1.03 (1H, m), 0.95 (3H, s), 0.85 (3H, t, J = 7.5 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.7, 135.0, 129.3, 113.8, 87.3, 57.8, 55.3, 45.6, 44.9, 40.8, 37.4, 33.2, 30.8, 23.2, 15.8, 13.3; HRMS [M + H]+ calculated for C18H29O2 277.2168, found 277.2186.

1-Methoxy-4-(2-(4-methoxy-2,2,3,3-tetramethylcyclobutyl)ethyl)benzene (29, trans). Colorless oil.

1


(3H, s), 3.13 (1H, d, J = 8.6 Hz), 2.51 (2H, t, J = 8.0 Hz), 1.90 (1H, dt, J = 8.0, 7.5 Hz), 1.70-1.63 (2H, m), 1.00 (3H, s), 0.99 (3H, s), 0.91 (6H, s); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 135.2, 129.3, 113.8, 86.7, 58.2, 55.4, 48.6, 42.6, 34.8, 33.9, 31.5, 24.6, 23.8, 20.8, 18.7; HRMS [M + H]+ calculated for C18H29O2 277.2168, found 277.2139.

(4-Methoxybut-3-en-1-yl)benzene (30, cis : trans = 1 : 1). Colorless oil.


34

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cis: 1H NMR (CDCl3, 500 MHz)  7.28 (2H, m), 7.18 (2H, d, J = 7.5 Hz), 7.17 (1H, tt, J = 8.0, 1.2 Hz), 5.87 (1H, dt, J = 6.3, 1.7 Hz), 4.37 (1H, dt, J = 6.9, 6.9 Hz), 3.55 (3H, s), 2.66 (2H, t, J = 7.5 Hz), 2.39 (2H, dq, J = 7.3, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  146.6, 142.4, 128.6, 128.3, 125.8, 106.1, 59.6, 36.1, 25.7. trans: 1H NMR (CDCl3, 500 MHz)  7.28 (2H, m), 7.20 (2H, d, J = 7.5 Hz), 7.17 (1H, dt, J = 8.0, 1.2 Hz), 6.30 (1H, dt, J = 12.6, 1.2 Hz), 4.76 (1H, dt, J = 12.6, 7.5 Hz), 3.49 (3H, s), 2.65 (2H, t, J = 8.0 Hz), 2.24 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  147.6, 142.1, 128.6, 128.4, 125.9, 102.3, 56.0, 37.6, 30.0; HRMS [M + H]+ calculated for C11H15O 163.1124, found 163.1095.

1-(4-Methoxybut-3-en-1-yl)-4-phenoxybenzene (31, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.31 (2H, dt, J = 8.0, 1.2 Hz), 7.17 (2H, d, J = 8.6 Hz), 7.07 (1H, dt, J = 7.5, 1.2 Hz), 6.98 (2H, d, J = 8.3 Hz), 6.93 (2H, d, J = 8.3 Hz), 5.89 (1H, dt, J = 6.3, 1.2 Hz), 4.37 (1H, dt, J = 6.9, 6.3 Hz), 3.56 (3H, s), 2.64 (2H, t, J = 7.5 Hz), 2.38 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.9, 155.1, 146.7, 137.5, 129.8, 129.8, 123.0, 119.1, 118.5, 106.0, 59.6, 35.3, 25.8. trans: 1H NMR (CDCl3, 500 MHz)  7.32 (2H, dt, J = 8.0, 1.2 Hz), 7.13 (2H, d, J = 8.6 Hz), 7.08 (1H, dt, J = 7.5, 1.2 Hz), 6.99 (2H, dd, J = 8.6, 1.2 Hz), 6.93 (2H, d, J = 8.0 Hz), 6.30 (1H, dt, J =


35


Page 36 of 59

12.6, 1.2 Hz), 4.75 (1H, dt, J = 12.6, 7.5 Hz), 3.50 (3H, s), 2.63 (2H, t, J = 8.0 Hz), 2.23 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  157.8, 155.2, 147.7, 137.1, 129.8, 123.1, 119.1, 118.6, 102.3, 56.1, 36.8, 30.1; HRMS [M + H]+ calculated for C17H19O2 255.1386, found 255.1368.

tert-Butyl(4-(4-methoxybut-3-en-1-yl)phenoxy)dimethylsilane (32, cis : trans = 1 : 1). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.04 (2H, d, J = 8.6 Hz), 6.74 (2H, d, J = 8.6 Hz), 5.86 (1H, dt, J = 5.7, 1.7 Hz), 4.35 (1H, dt, J = 7.5, 6.3 Hz), 3.55 (3H, s), 2.58 (2H, t, J = 7.5 Hz), 2.34 (2H, dq, J = 7.5, 1.2 Hz), 0.97 (9H, s), 0.17 (6H, s);

13

C{1H} NMR (125 MHz, CDCl3)  153.6, 146.4,

135.1, 129.4, 119.8, 106.2, 59,6, 35.3, 30.1, 25.8, 18.3, -4.3. trans: 1H NMR (CDCl3, 500 MHz)  7.01 (2H, d, J = 8.0 Hz), 6.75 (2H, d, J = 8.6 Hz), 6.28 (1H, dt, J = 12.6, 1.2 Hz), 4.73 (1H, dt, J = 12.6, 7.5 Hz), 3.48 (3H, s), 2.57 (2H, t, J = 8.0 Hz), 2.19 (2H, dq, J = 7.5, 1.2 Hz), 0.97 (9H, s), 0.18 (6H, s); 13C{1H} NMR (125 MHz, CDCl3)  153.7, 147.5, 134.8, 129.4, 119.9, 102.4, 55.9, 36.7, 30.1, 25.9, 25.8, -4.3; HRMS [M + H]+ calculated for C17H29O2Si 293.1938, found 293.1945.

4-(4-Methoxybut-3-en-1-yl)phenol (33, cis : trans = 1 : 1). Colorless oil.


36

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cis: 1H NMR (CDCl3, 500 MHz)  7.04 (2H, d, J = 8.0 Hz), 6.73 (2H, d, J = 8.0 Hz), 5.87 (1H, dt, J = 6.3, 1.7 Hz), 4.37 (1H, dt, J = 7.5, 6.3 Hz), 3.55 (3H, s), 2.57 (2H, t, J = 6.9 Hz), 2.34 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  153.7, 146.3, 134.4, 129.6, 115.2, 106.5, 59.6, 35.1, 25.9. trans: 1H NMR (CDCl3, 500 MHz)  7.02 (2H, d, J = 8.6 Hz), 6.74 (2H, d, J = 8.6 Hz), 6.28 (1H, dt, J = 12.6, 1.2 Hz), 4.77 (1H, dt, J = 12.6, 7.5 Hz), 3.49 (3H, s), 2.56 (2H, t, J = 8.0 Hz), 2.18 (2H, dq, J = 8.0, 1.3 Hz); 13C{1H} NMR (125 MHz, CDCl3)  153.8, 147.2, 134.1, 129.7, 115.3, 102.9, 56.1, 36.5, 30.1; HRMS [M + H]+ calculated for C11H15O2 179.1073, found 179.1063.


cis: 1H NMR (CDCl3, 500 MHz)  7.17 (1H, dt, J = 8.0, 1.7 Hz), 7.15 (1H, d, J = 6.9 Hz), 6.87 (1H, dt, J = 6.9, 1.2 Hz), 6.83 (1H, d, J = 8.0 Hz), 5.86 (1H, dt, J = 6.3, 1.2 Hz), 4.38 (1H, dt, J = 7.5, 6.3 Hz), 3.82 (3H, s), 3.55 (3H, s), 2.66 (2H, t, J = 6.9 Hz), 2.37 (2H, dq, J = 7.5, 1.2 Hz); C{1H} NMR (125 MHz, CDCl3)  157.7, 146.3, 130.7, 129.9, 127.0, 120.3, 110.3, 106.7, 59.5,

13

55.3, 30.3, 24.0.


37


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trans: 1H NMR (CDCl3, 500 MHz)  7.17 (1H, dt, J = 8.0, 1.7 Hz), 7.12 (1H, dd, J = 6.9, 1.2 Hz), 6.87 (1H, dt, J = 6.9, 1.2 Hz), 6.84 (1H, d, J = 8.0 Hz), 6.30 (1H, d, J = 12.6 Hz), 4.78 (1H, dt, J = 12.6, 7.5 Hz), 3.82 (3H, s), 3.49 (3H, s), 2.65 (2H, t, J = 8.0 Hz), 2.20 (2H, dq, J = 7.5, 1.2 Hz); C{1H} NMR (125 MHz, CDCl3)  147.3, 130.5, 129.9, 127.1, 120.4, 110.3, 102.9, 55.9, 55.3,

13

31.9, 28.2; HRMS [M + H]+ calculated for C12H17O2 193.1229, found 193.1204.


cis: 1H NMR (CDCl3, 500 MHz)  7.20 (1H, t, J = 7.5 Hz), 6.80 (1H, d, J = 7.5 Hz), 6.75-6.71 (2H, m), 5.87 (1H, dt, J = 6.3, 1.2 Hz), 4.36 (1H, dt, J = 7.5, 6.3 Hz), 3.79 (3H, s), 3.56 (3H, s), 2.64 (2H, t, J = 6.9 Hz), 2.39 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  159.7, 146.6, 144.1, 129.3, 121.1, 114.3, 111.2, 106.1, 59.8, 56.1, 36.1, 25.6. trans: 1H NMR (CDCl3, 500 MHz)  7.18 (1H, t, J = 7.5 Hz), 6.77 (1H, d, J = 7.5 Hz), 6.75-6.71 (2H, m), 6.31 (1H, dt, J = 12.6, 1.2 Hz), 4.75 (1H, dt, J = 12.6, 7.5 Hz), 3.80 (3H, s), 3.49 (3H, s), 2.63 (2H, t, J = 6.3 Hz), 2.24 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  159.8, 147.7, 143.8, 129.4, 121.1, 114.4, 111.2, 102.4, 59.8, 55.3, 37.6, 29.8; HRMS [M + H]+ calculated for C12H17O2 193.1229, found 193.1210.


38

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2,4-Dimethoxy-1-(4-methoxybut-3-en-1-yl)benzene (36, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.05 (1H, d, J = 8.0 Hz), 6.43 (1H, d, J = 2.9 Hz), 6.41 (1H, dd, J = 8.0, 2.3 Hz), 5.86 (1H, dt, J = 6.3, 1.2 Hz), 4.37 (1H, dt, J = 7.5, 6.3 Hz), 3.79 (3H, s), 3.79 (3H, s), 3.56 (3H, s), 2.59 (2H, t, J = 7.5 Hz), 2.33 (2H, dq, J = 7.5, 1.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  159.1, 158.4, 146.2, 129.9, 123.0, 106.7, 103.7, 98.4, 59.4, 55.2, 55.2, 29.6, 24.1. trans: 1H NMR (CDCl3, 500 MHz)  7.01 (1H, d, J = 8.0 Hz), 6.44 (1H, d, J = 2.3 Hz), 6.41 (1H, dd, J = 8.0, 2.3 Hz), 6.29 (1H, dt, J = 12.6, 1.4 Hz), 4.77 (1H, dt, J = 12.6, 7.5 Hz), 3.79 (3H, s), 3.79 (3H, s), 3.49 (3H, s), 2.58 (2H, t, J = 8.0 Hz), 2.16 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  159.2, 158.3, 147.2, 130.1, 122.7, 103.7, 102.8, 98.4, 55.7, 55.2, 55.1, 31.2, 28.4; HRMS [M + H]+ calculated for C13H19O3 223.1335, found 223.1357.

1,3,5-Trimethoxy-2-(4-methoxybut-3-en-1-yl)benzene (37, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  6.12 (2H, s), 5.83 (1H, dt, J = 6.3, 1.7 Hz), 4.40 (1H, dt, J = 7.5, 6.3 Hz), 3.80 (3H, s), 3.79 (6H, s), 3.54 (3H, s), 2.61 (2H, t, J = 7.5 Hz), 2.23 (2H, dq, J = 7.5,


39


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1.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  159.3, 159.0, 145.8, 111.5, 107.5, 90.6, 59.5, 55.8, 55.3, 23.9, 22.8. trans: 1H NMR (CDCl3, 500 MHz)  6.28 (1H, d, J = 12.6 Hz), 6.12 (2H, s), 4.80 (1H, dt, J = 12.6, 7.5 Hz), 3.80 (3H, s), 3.79 (6H, s), 3.49 (3H, s), 2.59 (2H, t, J = 8.0 Hz), 2.05 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  159.3, 158.9, 146.9, 111.1, 103.5, 90.5, 59.5, 55.6, 55.3, 27.8, 24.1; HRMS [M + H]+ calculated for C14H21O4 253.1441, found 253.1468.

1,2-Dimethoxy-4-(4-methoxybut-3-en-1-yl)benzene (38, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  6.80 (1H, d, J = 3.7 Hz), 6.76-6.72 (1H, m), 6.72-6.70 (1H, m), 5.88 (1H, dt, J = 5.7, 1.2 Hz), 4.37 (1H, dt, J = 7.5, 6.3 Hz), 3.88 (3H, s), 3.85 (3H, s), 3.57 (3H, s), 2.61 (2H, t, J = 7.5 Hz), 2.37 (2H, dq, J = 7.5, 1.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  148.5, 146.9, 146.3, 134.9, 120.2, 111.7, 111.0, 105.9, 55.8, 55.8, 55.6, 35.4, 25.6. trans: 1H NMR (CDCl3, 500 MHz)  6.78 (1H, s), 6.76-6.72 (1H, m), 6.72-6.70 (1H, m), 6.31 (1H, dt, J = 12.6, 1.2 Hz), 4.75 (1H, dt, J = 12.6, 6.9 Hz), 3.88 (3H, s), 3.86 (3H, s), 3.49 (3H, s), 2.60 (2H, t, J = 7.5 Hz), 2.22 (2H, dq, J = 7.5, 1.2 Hz);

13

C{1H} NMR (125 MHz, CDCl3)  148.6,

147.3, 147.0, 134.6, 120.3, 111.8, 111.1, 102.2, 55.8, 55.8, 55.6, 36.9, 29.9; HRMS [M + H]+ calculated for C13H19O3 223.1335, found 223.1319.


40

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1,2,3-Trimethoxy-5-(4-methoxybut-3-en-1-yl)benzene (39, cis : trans = 1 : 1). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  6.43 (1H, s), 6.40 (1H, s), 5.90 (1H, dt, J = 6.3, 1.7 Hz), 4.37 (1H, dt, J = 7.5, 6.3 Hz), 3.85 (6H, s), 3.82 (3H, s), 3.58 (3H, s), 2.61 (2H, t, J = 8.6 Hz), 2.39 (2H, dq, J = 7.5, 1.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  152.9, 147.5, 137.8, 135.9, 105.3, 102.1, 59.5, 56.0, 55.9, 37.8, 25.5. trans: 1H NMR (CDCl3, 500 MHz)  6.43 (1H, s), 6.40 (1H, s), 6.33 (1H, dt, J = 12.6, 1.1 Hz), 4.76 (1H, dt, J = 12.6, 7.5 Hz), 3.85 (6H, s), 3.83 (3H, s), 3.50 (3H, s), 2.60 (2H, t, J = 8.0 Hz), 2.24 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  153.0, 146.5, 138.1, 136.0, 105.8, 105.2, 60.8, 56.0, 55.9, 36.3, 29.9; HRMS [M + H]+ calculated for C14H21O4 253.1441, found 253.1456.

1-(4-Methoxybut-3-en-1-yl)-4-methylbenzene (40, cis : trans = 1 : 1). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.11-7.05 (4H, m), 5.87 (1H, dt, J = 6.3, 1.2 Hz), 4.36 (1H, dt, J = 6.9, 6.3 Hz), 3.56 (3H, s), 2.62 (2H, t, J = 7.5 Hz), 2.37 (2H, dq, J = 7.5, 1.2 Hz), 2.31 (3H, s);


41


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C{1H} NMR (125 MHz, CDCl3)  146.5, 139.3, 135.2, 129.0, 128.5, 106.2, 59.6, 35.6, 30.1,

13

21.2. trans: 1H NMR (CDCl3, 500 MHz)  7.11-7.05 (4H, m), 6.30 (1H, dt, J = 12.6, 1.2 Hz), 4.75 (1H, dt, J = 12.6, 7.5 Hz), 3.49 (3H, s), 2.61 (2H, t, J = 8.0 Hz), 2.32 (3H, s), 2.21 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  147.5, 139.0, 135.3, 129.1, 128.5, 102.5, 56.0, 37.1, 25.8, 21.2; HRMS [M + H]+ calculated for C12H17O 177.1280, found 177.1266.

1-(4-Methoxybut-3-en-1-yl)-2,4-dimethylbenzene (41, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.05 (1H, d, J = 8.0 Hz), 6.97-6.92 (2H, m), 5.89 (1H, dt, J = 6.3, 1.5 Hz), 4.40 (1H, dt, J = 7.5, 6.3 Hz), 3.57 (3H, s), 2.60 (2H, t, J = 7.5 Hz), 2.32 (2H, q, J = 7.5 Hz), 2.28 (3H, s), 2.28 (3H, s); 13C{1H} NMR (125 MHz, CDCl3)  146.6, 137.5, 136.0, 135.3, 131.0, 128.8, 126.6, 106.3, 59.6, 33.0, 24.6, 21.0, 19.4. trans: 1H NMR (CDCl3, 500 MHz)  7.02 (1H, d, J = 7.5 Hz), 6.97-6.92 (2H, m), 6.33 (1H, d, J = 12.6 Hz), 4.79 (1H, dt, J = 12.6, 7.5 Hz), 3.50 (3H, s), 2.60 (2H, t, J = 7.5 Hz), 2.28 (3H, s), 2.27 (3H, s), 2.17 (2H, q, J = 7.5 Hz); 13C{1H} NMR (125 MHz, CDCl3)  147.5, 137.2, 135.8, 135.4, 131.1, 129.0, 126.7, 102.7, 56.0, 34.5, 28.9, 21.0, 19.4; HRMS [M + H]+ calculated for C13H19O 191.1437, found 191.1448.


42

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2-(4-Methoxybut-3-en-1-yl)-1,3,5-trimethylbenzene (42, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  6.82 (2H, s), 5.91 (1H, dt, J = 6.3, 1.2 Hz), 4.45 (1H, dt, J = 7.5, 6.3 Hz), 3.58 (3H, s), 2.62 (2H, t, J = 8.6 Hz), 2.31 (6H, s), 2.24 (3H, s), 2.20 (2H, dq, J = 6.9, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  146.7, 136.2, 135.8, 134.9, 128.9, 106.5, 59.6, 29.8, 23.8, 20.0, 19.8. trans: 1H NMR (CDCl3, 500 MHz)  6.83 (2H, s), 6.36 (1H, dt, J = 12.6, 1.2 Hz), 4.82 (1H, dt, J = 12.6, 7.5 Hz), 3.52 (3H, s), 2.62 (2H, t, J = 8.0 Hz), 2.29 (6H, s), 2.24 (3H, s), 2.07 (2H, dq, J = 6.9, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  147.4, 136.3, 136.1, 135.1, 129.1, 102.8, 56.0, 31.1, 27.7, 21.0, 20.0; HRMS [M + H]+ calculated for C14H21O 205.1593, found 205.1564.

(4-(4-Methoxybut-3-en-1-yl)phenyl)(methyl)sulfane (43, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.19 (2H, d, J = 8.6 Hz), 7.13 (2H, d, J = 8.6 Hz), 5.87 (1H, dt, J = 6.0, 1.2 Hz), 4.34 (1H, dt, J = 7.5, 6.3 Hz), 3.56 (3H, s), 2.62 (2H, t, J = 6.9 Hz), 2.46 (3H, s), 2.36 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  146.6, 139.6, 135.1, 129.1, 127.2, 105.8, 59.6, 35.5, 25.6, 16.5.


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trans: 1H NMR (CDCl3, 500 MHz)  7.20 (2H, d, J = 8.0 Hz), 7.10 (2H, d, J = 8.6 Hz), 6.29 (1H, dt, J = 12.6, 1.2 Hz), 4.73 (1H, dt, J = 12.6, 6.9 Hz), 3.49 (3H, s), 2.61 (2H, t, J = 8.0 Hz), 2.47 (3H, s), 2.21 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  147.7, 139.2, 135.3, 129.2, 127.2, 102.1, 56.0, 37.0, 29.8, 16.4; HRMS [M + H]+ calculated for C12H17OS 209.1001, found 209.0080.

4-(4-Methoxybut-3-en-1-yl)-N,N-dimethylaniline (44, cis : trans = 1 : 2). Colorless oil.

cis: 1H NMR (CDCl3, 500 MHz)  7.09 (2H, d, J = 8.6 Hz), 6.70 (2H, d, J = 8.6 Hz), 5.87 (1H, dt, J = 5.7, 1.2 Hz), 4.37 (1H, dt, J = 7.5, 6.3 Hz), 3.56 (3H, s), 2.90 (6H, s), 2.57 (2H, t, J = 6.9 Hz), 2.35 (2H, dq, J = 7.5, 1.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  149.1, 146.3, 130.7, 129.1, 113.1, 106.5, 59.6, 41.1, 35.1, 26.0. trans: 1H NMR (CDCl3, 500 MHz)  7.06 (2H, d, J = 8.6 Hz), 6.70 (2H, d, J = 8.6 Hz), 6.31 (1H, dt, J = 12.6, 1.3 Hz), 4.77 (1H, dt, J = 12.6, 7.5 Hz), 3.49 (3H, s), 2.91 (6H, s), 2.55 (2H, t, J = 6.9 Hz), 2.19 (2H, dq, J = 7.5, 1.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  149.2, 147.4, 130.4, 129.2, 113.1, 102.7, 56.0, 41.0, 36.5, 30.3; HRMS [M + H]+ calculated for C13H20NO 206.1546, found 206.1573.

1-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)-4-phenoxybenzene (46, all trans). Colorless oil.


44

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1

H NMR (CDCl3, 500 MHz) δ 7.32 (1H, d, J = 8.6 Hz), 7.31 (1H, d, J = 8.6 Hz), 7.13 (2H, d, J =

8.0 Hz), 7.07 (1H, tt, J = 7.5, 1.2 Hz), 6.98 (2H, d, J = 8.0 Hz), 6.92 (2H, d, J = 8.6 Hz), 3.31 (3H, s), 3.11 (1H, t, J = 6.9 Hz), 2.61-2.50 (2H, m), 2.07-1.87 (4H, m), 1.67-1.55 (2H, m), 1.36-1.19 (5H, m), 0.89 (3H, t, J = 7.5 Hz), 0.73 (1H, q, J = 9.2 Hz); 13C{1H} NMR (125 MHz, CDCl3) δ 157.9, 155.1, 137.7, 129.8, 129.7, 123.0, 119.2, 118.6, 86.6, 56.6, 40.7, 40.2, 37.4, 35.2, 33.1, 29.8, 25.6, 22.9, 14.3; HRMS [M + H]+ calculated for C23H31O2 339.2325, found 339.2295.

tert-Butyl(4-(2-(3-butyl-2-methoxycyclobutyl)ethyl)phenoxy)dimethylsilane

(47,

all

trans).

Colorless oil.

1


(1H, t, J = 6.9 Hz), 2.56-2.44 (2H, m), 2.05-1.83 (4H, m), 1.63-1.53 (2H, m), 1.34-1.18 (5H, m), 0.97 (9H, s), 0.88 (3H, t, J = 6.9 Hz), 0.70 (1H, q, J = 9.7 Hz), 0.18 (6H, s); 13C{1H} NMR (125 MHz, CDCl3)  153.7, 135.4, 129.3, 119.9, 86.6, 56.6, 40.7, 40.3, 37.5, 35.1, 33.1, 29.8, 25.9, 25.6, 22.9, 18.4, 14.3, -4.3; HRMS [M + H]+ calculated for C23H41O2Si 377.2877, found 377.2869.


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4-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)phenol (48, all trans). Colorless oil.

1


(1H, t, J = 6.9 Hz), 2.56-2.43 (2H, m), 2.06-1.92 (3H, m), 1.92-1.83 (1H, m), 1.62-1.53 (2H, m), 1.35-1.18 (5H, m), 0.88 (3H, t, J = 6.9 Hz), 0.71 (1H, q, J = 9.2 Hz); 13C{1H} NMR (125 MHz, CDCl3)  153.8, 134.7, 129.5, 86.6, 6.6, 40.7, 40.1, 37.5, 35.1, 32.9, 29.8, 2.6, 22.9, 14.3; HRMS [M + H]+ calculated for C17H27O2 263.2012, found 263.2030.


1

H NMR (CDCl3, 500 MHz)  7.15 (1H, dt, J = 7.5, 1.7 Hz), 7.11 (1H, dd, J = 7.5, 1.7 Hz), 6.86

(1H, t, J = 7.5 Hz), 6.82 (1H, d, J = 8.0 Hz), 3.81 (3H, s), 3.30 (3H, s), 3.11 (1H, t, J = 6.9 Hz), 2.62-2.51 (2H, m), 2.08-1.84 (4H, m), 1.63-1.53 (2H, m), 1.36-1.19 (5H, m), 0.88 (3H, t, J = 6.9 Hz), 0.73 (1H, q, J = 9.7 Hz);

13

C{1H} NMR (125 MHz, CDCl3)  157.6, 131.1, 129.9, 127.0,

120.5, 110.4, 86.7, 56.6, 55.4, 40.7, 40.6, 35.6, 35.1, 29.8, 28.2, 25.6, 22.9, 14.2; HRMS [M + H]+ calculated for C18H29O2 277.2168, found 277.2177.


46

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1

H NMR (CDCl3, 500 MHz)  7.19 (1H, dd, J = 8.6, 7.5 Hz), 6.77 (1H, d, J = 8.0 Hz), 6.74-6.71

(2H, m), 3.80 (3H, s), 3.30 (3H, s), 3.11 (1H, t, J = 6.9 Hz), 2.61-2.48 (2H, m), 2.08-1.87 (4H, m), 1.66-1.54 (2H, m), 1.36-1.17 (5H, m), 0.88 (3H, t, J = 6.9 Hz), 0.73 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  159.7, 144.3, 129.4, 120.9, 114.3, 111.1, 86.5, 56.6, 55.3, 40.7, 40.2, 37.3, 35.2, 33.9, 29.8, 25.6, 22.9, 14.3; HRMS [M + H]+ calculated for C18H29O2 277.2168, found 277.2145.

1-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)-2,4-dimethoxybenzene (51, all trans). Colorless oil.

1

H NMR (CDCl3, 500 MHz)  7.01 (1H, d, J = 8.0 Hz), 6.43 (1H, d, J = 2.9 Hz), 6.40 (1H, dd, J

= 7.5, 2.9 Hz), 3.79 (6H, s), 3.31 (3H, s), 3.10 (1H, t, J = 6.9 Hz), 2.55-2.43 (2H, m), 2.07-1.90 (3H, m), 1.88-1.80 (1H, m), 1.60-1.51 (2H, m), 1.36-1.19 (5H, m), 0.88 (3H, t, J = 6.8 Hz), 0.72 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  169.1, 158.4, 130.0, 123.4, 103.8, 98.6,


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86.7, 56.6, 55.5, 55.4, 40.7, 40.6, 35.9, 35.1, 29.8, 27.5, 25.6, 22.9, 14.3; HRMS [M + H]+ calculated for C19H31O3 307.2274, found 307.2284.

4-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)-1,2-dimethoxybenzene (53, all trans). Colorless oil.

Inseparable Mixtures. HRMS [M + H]+ calculated for C19H31O3 307.2274, found 307.2256

1-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)-4-methylbenzene (55, all trans). Colorless oil.

1

H NMR (CDCl3, 500 MHz)  7.11-7.04 (4H, m), 3.30 (3H, s), 3.11 (1H, t, J = 6.8 Hz), 2.58-2.47

(2H, m), 2.31 (3H, s), 2.07-1.85 (4H, m), 1.65-1.52 (2H, m), 1.36-1.20 (5H, m), 0.88 (3H, t, J = 7.5 Hz), 0.72 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  139.6, 135.2, 129.1, 128.3, 86.6, 56.6, 40.7, 40.3, 37.5, 35.1, 33.4, 29.8, 25.6, 22.9, 21.2, 14.3; HRMS [M + H]+ calculated for C18H29O 261.2219, found 261.2244.


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1-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)-2,4-dimethylbenzene (56, all trans). Colorless oil.

1

H NMR (CDCl3, 500 MHz)  7.01 (1H, d, J = 7.5 Hz), 6.96-6.91 (2H, m), 3.31 (3H, s), 3.11 (1H,

t, J = 7.5 Hz), 2.54-2.45 (2H, m), 2.28 (3H, s), 2.26 (3H, s), 2.10-1.92 (3H, m), 1.87-1.79 (1H, m), 1.61-1.50 (2H, m), 1.37-1.19 (5H, m), 0.88 (3H, t, J = 7.5 Hz), 0.74 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  137.7, 135.7, 135.3, 131.1, 128.8, 126.7, 86.6, 56.7, 40.7, 40.6, 36.3, 35.2, 30.8, 29.8, 25.7, 22.9, 21.0, 19.3, 14.2; HRMS [M + H]+ calculated for C19H31O 275.2376, found 275.2387.

2-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)-1,3,5-trimethylbenzene (57, all trans). Colorless oil.

1

H NMR (CDCl3, 500 MHz)  6.82 (2H, s), 3.32 (3H, s), 3.11 (1H, t, J = 6.9 Hz), 2.52 (2H, t, J =

8.6 Hz), 2.27 (6H, s), 2.23 (3H, s), 2.15-1.93 (3H, m), 1.75-1.67 (1H, m), 1.63-1.55 (1H, m), 1.491.18 (6H, m), 0.89 (3H, t, J = 6.9 Hz), 0.77 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  136.3, 135.9, 135.0, 129.0, 86.6, 56.7, 41.2, 40.8, 35.2, 34.9, 29.8, 27.3, 25.6, 22.9, 20.9, 19.8, 14.3; HRMS [M + H]+ calculated for C20H33O 289.2532, found 289.2533.


49


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(4-(2-(3-Butyl-2-methoxycyclobutyl)ethyl)phenyl)(methyl)sulfane (58, all trans). Colorless oil.

1


(1H, t, J = 6.9 Hz), 2.58-2.47 (2H, m), 2.46 (3H, s), 2.05-1.83 (4H, m), 1.65-1.53 (2H, m), 1.351.19 (5H, m), 0.88 (3H, t, J = 6.9 Hz), 0.71 (1H, q, J = 9.7 Hz); 13C{1H} NMR (125 MHz, CDCl3)  139.9, 135.2, 129.1, 127.4, 86.6, 56.6, 40.8, 40.2, 37.3, 35.1, 33.3, 29.8, 25.6, 22.9, 16.6, 14.2; HRMS [M + H]+ calculated for C18H29OS 293.1940, found 293.1957.

Theoretical Calculations: Structure optimizations of all stationary points and frequency analyses were carried out at the B3LYP level of density functional theory (DFT) with the 6-311G++(2d,2p) basis set in nitromethane (PCM model). No imaginary frequency was observed for all compounds.

ASSOCIATED CONTENT AUTHOR INFORMATION Corresponding Author *[email protected]


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Notes The authors declare no competing financial interest. ACKNOWLEDGMENT This work was partially supported by JSPS KAKENHI Grant Numbers 16H06193, 17K19221 (to Y. O.), and 16H02413 (to H. K.). Supporting Information. Additional figures and tables, and copies of 1H and

13

C{1H} NMR

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