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On acidification of thiols to produce the corresponding disulfides
Abd El-Wareth A. O. Sarhan,
Corresponding Author
Abd El-Wareth A. O. Sarhan
Chemistry Department, Faculty of Science, Assiut University Assiut 71516, Egypt
Chemistry Department, Faculty of Science, Assiut University Assiut 71516, EgyptSearch for more papers by this authorAbd El-Wareth A. O. Sarhan,
Corresponding Author
Abd El-Wareth A. O. Sarhan
Chemistry Department, Faculty of Science, Assiut University Assiut 71516, Egypt
Chemistry Department, Faculty of Science, Assiut University Assiut 71516, EgyptSearch for more papers by this authorFirst published: 14 November 2000
Citations: 6
Abstract
Thiophenol 1, 2-mercaptobenzimidazole (3a), 4,5-diphenylimidazole-2-thione 3b, and 5-mercapto-2-aryl-1,2,4-s-triazoles (6a–b) are chemically oxidized using the acidified acetic acid method to the corresponding disulfides 2, 5a–b and 7a–b, respectively. The structures of the disulfides thus formed were established both chemically and by spectral analysis. © 2000 John Wiley & Sons, Inc. Heteroatom Chem 16:399–402, 2000
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