Thiolate-Disulfide Interchange

Bibliographic References tagged with Thiolate-Disulfide Interchange

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P. J. Bracher, P. W. Snyder, B. R. Bohall, and G. M. Whitesides. 2011. “The Relative Rates of Thiol-Thioester Exchange and Hydrolysis for Alkyl and Aryl Thioalkanoates in Water”. Origins Life Evol. Biosph., 41, Pp. 399-412
P. J. Bracher, P. W. Snyder, B. R. Bohall, and G. M. Whitesides. 2011. “The Relative Rates of Thiol-Thioester Exchange and Hydrolysis for Alkyl and Aryl Thioalkanoates in Water”. Origins Life Evol. Biosph., 41, Pp. 399-412
J. Houk and G. M. Whitesides. 1989. “Characterization and Stability of Cyclic Disulfides and Cyclic Dimeric Bis(disulfides)”. Tetrahedron, 45, Pp. 91-102
J. Houk and G. M. Whitesides. 1989. “Characterization and Stability of Cyclic Disulfides and Cyclic Dimeric Bis(disulfides)”. Tetrahedron, 45, Pp. 91-102
R. Singh and G. M. Whitesides. 1990. “Comparison of Rate Constants for Thiolate-Disulfide Interchange in Water and in Polar Aprotic Solvents Using Dynamic 1H NMR Line Shape Analysis”. J. Am. Chem. Soc., 112, Pp. 1190-97
R. Singh and G. M. Whitesides. 1990. “Comparison of Rate Constants for Thiolate-Disulfide Interchange in Water and in Polar Aprotic Solvents Using Dynamic 1H NMR Line Shape Analysis”. J. Am. Chem. Soc., 112, Pp. 1190-97
J. A. Burns and G. M. Whitesides. 1990. “Predicting the Stability of Cyclic Disulfides by Molecular Modeling: ’Effective Concentrations’ in Thiol-Disulfide Interchange and the Design of Strongly Reducing Dithiols”. J. Am. Chem. Soc., 112, Pp. 6296-6303
J. A. Burns and G. M. Whitesides. 1990. “Predicting the Stability of Cyclic Disulfides by Molecular Modeling: ’Effective Concentrations’ in Thiol-Disulfide Interchange and the Design of Strongly Reducing Dithiols”. J. Am. Chem. Soc., 112, Pp. 6296-6303
R. Singh and G. M. Whitesides. 1990. “Degenerate Intermolecular Thiolate-Disulfide Interchange Involving Cyclic Five-Membered Disulfides Is Faster by ~103 Than That Involving Six- or Seven-Membered Disulfides”. J. Am. Chem. Soc., 112, Pp. 6304-9
R. Singh and G. M. Whitesides. 1990. “Degenerate Intermolecular Thiolate-Disulfide Interchange Involving Cyclic Five-Membered Disulfides Is Faster by ~103 Than That Involving Six- or Seven-Membered Disulfides”. J. Am. Chem. Soc., 112, Pp. 6304-9
R. Singh and G. M. Whitesides. 1991. “A Reagent for Reduction of Disulfide Bonds in Proteins That Reduces Disulfide Bonds Faster Than Does Dithiothreitol”. J. Org. Chem., 56, Pp. 2332-37
R. Singh and G. M. Whitesides. 1991. “A Reagent for Reduction of Disulfide Bonds in Proteins That Reduces Disulfide Bonds Faster Than Does Dithiothreitol”. J. Org. Chem., 56, Pp. 2332-37
J. A. Burns, J. C. Butler, J. R. Moran, and G. M. Whitesides. 1991. “Selective Reduction of Disulfides by Tris(2-Carboxyethyl)phosphine”. J. Org. Chem., 56, Pp. 2648-50
J. A. Burns, J. C. Butler, J. R. Moran, and G. M. Whitesides. 1991. “Selective Reduction of Disulfides by Tris(2-Carboxyethyl)phosphine”. J. Org. Chem., 56, Pp. 2648-50
R. Singh and G. M. Whitesides. 1991. “Selenols Catalyze the Interchange Reactions of Dithiols and Disulfides in Water”. J. Org. Chem., 56, Pp. 6931-33
R. Singh and G. M. Whitesides. 1991. “Selenols Catalyze the Interchange Reactions of Dithiols and Disulfides in Water”. J. Org. Chem., 56, Pp. 6931-33
W. J. Lees, R. Singh, and G. M. Whitesides. 1991. “Meso-2,5-Dimercapto-N,N,N’,N’-Tetramethyladipamide: A Readily Available, Kinetically Rapid Reagent for the Reduction of Disulfides in Aqueous Solution”. J. Org. Chem., 56, Pp. 7328-31
W. J. Lees, R. Singh, and G. M. Whitesides. 1991. “Meso-2,5-Dimercapto-N,N,N’,N’-Tetramethyladipamide: A Readily Available, Kinetically Rapid Reagent for the Reduction of Disulfides in Aqueous Solution”. J. Org. Chem., 56, Pp. 7328-31
W. J. Lees and G. M. Whitesides. 1993. “Interpretation of the Reduction Potential of 6,6’-Dideoxy-6,6’-Dithiosucrose Disulfide by Comparison of the Conformations of 6,6’-Dideoxy-6,6’-Dithiosucrose Disulfide, 6,6’-Dideoxysucrose-6,6’-Dithiol, and Sucrose in Aqueous Solution”. J. Am. Chem. Soc., 115, Pp. 1860-69
W. J. Lees and G. M. Whitesides. 1993. “Interpretation of the Reduction Potential of 6,6’-Dideoxy-6,6’-Dithiosucrose Disulfide by Comparison of the Conformations of 6,6’-Dideoxy-6,6’-Dithiosucrose Disulfide, 6,6’-Dideoxysucrose-6,6’-Dithiol, and Sucrose in Aqueous Solution”. J. Am. Chem. Soc., 115, Pp. 1860-69