Radiation-induced "hydrolysis" of the peptide bond. Michael A. J. Rodgers, Harvey A. Sokol, Warren M. Garrison. J. Am. Chem. Soc. , 1968, 90 (3), pp 7...
May 1, 2002 - Michael A. J. Rodgers, Harvey A. Sokol, and Warren M. Garrison. J. Am. Chem. Soc. , 1968, 90 (3), pp 795â796. DOI: 10.1021/ja01005a045.
8 hours ago - A detailed quantum-chemical study combined with experimental data allowed to unravel the role of the {Zr6O8} core of MOF-808 in accelerating Gly-Gly hy-drolysis. A mechanism for the hydrolysis of Gly-Gly by MOF-808 is proposed in which
15 hours ago - MOF-808, a Zr(IV)-based metal-organic framework, has been proven to be a very effective heterogeneous catalyst for the hydrolysis of the peptide bond in a wide range of peptides and in hen egg white lysozyme protein. The kinetic experi
Apr 23, 2018 - MOF-808, a Zr(IV)-based metalâorganic framework, has been proven to be a very effective heterogeneous catalyst for the hydrolysis of the ...
Apr 23, 2018 - (20) These studies showed excellent catalytic performance of Zr-MOFs; however, to the best of our knowledge there is only one recent report in which hydrolysis of a .... Powder X-ray Diffraction (PXRD) was performed on a STOE STADI P C
Aug 21, 1998 - To analyze the data at pH 0, 1, and 14, exact analytic solutions were ... 10-6 M-1 s-1, a value nearly identical to k1 and k3 at this pH; at pH 0, k2 ...
The protein hydrolysis mechanism by the HIV-1 protease (HIV-1 PR) was studied using ab initio molecular orbital calculations with a model compound.
Jan 5, 2008 - View: PDF | PDF w/ Links | Full Text HTML ... Å afaÅÃk , MiloÅ¡ BudÄÅ¡Ãnský , MiloÅ¡ Tichý , Lucie Bednárová , VladimÃr Baumruk , and Petr MaloÅ.
J. Am. Chem. Soc. , 1961, 83 (15), pp 3180â3184. DOI: 10.1021/ja01476a003. Publication Date: August 1961. ACS Legacy Archive. Note: In lieu of an abstract, ...
Publication Date: August 1961. ACS Legacy Archive. Cite this:J. Am. Chem. Soc. 83, 15, 3180-3184. Note: In lieu of an abstract, this is the article's first page.
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initial scans the current peaks due to the oxidation of I successively decrease in amplitude (due t o exhaustion of I near the electrode), while those due to the redox couple of I1 increase (as the concentration of I1 builds up near the electrode). This demonstration of the oxidative coupling of I to form I1 is also observable in acetonitrile. A surprising fact about the reversible redox couple for I1 is that it is a two-electron process, This was clearly demonstrated by cyclic coulometry. Closely related to this tetraaminobutadiene is tetrakis(dimethy1amino)ethylene (111) which was studied extensively by Kuwata and Geske.6 The cyclic voltammetry of I11 appears in Figure 3. Note that the two one-electron steps are separated by only 0.1 v for this compound. We are presently studying the electrolytic oxidations of other aminoethylenes and of aromatic hydrocarbons and will report on these in the near future. (5) I
