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Synthesis and Biological Evaluation of Diastereomeric (E and Z) Sulfides, Sulfones, Sulfide-Sulfones, and Disulfones

The addition of p-chlorobenzenethiol to benzyl p-chlorophenylketone resulted in the formation of a mixture of diastereomers (E)- and (Z)-1-p-chlorophenyl-2-phenyl-1-p-chlorophenylthioethylene (1 and 2). These compounds, upon reaction with bromine in acetic acid, yielded a mixture of (E)- and (Z)-1-b...

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Published in:Phosphorus, sulfur, and silicon and the related elements sulfur, and silicon and the related elements, 2011-08, Vol.186 (8), p.1721-1732
Main Authors: Reddy, A. Babul, Hymavathi, A., Kumar, L. Vinay, Penchalaiah, N., Naik, P. Jagan, Naveen, M., Swamy, G. Narayana
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container_title Phosphorus, sulfur, and silicon and the related elements
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description The addition of p-chlorobenzenethiol to benzyl p-chlorophenylketone resulted in the formation of a mixture of diastereomers (E)- and (Z)-1-p-chlorophenyl-2-phenyl-1-p-chlorophenylthioethylene (1 and 2). These compounds, upon reaction with bromine in acetic acid, yielded a mixture of (E)- and (Z)-1-bromo-2-p-chlorophenyl-1-phenyl-2-p-chlorophenylthioethylenes (5a and 5b). Oxidation of 5a and 5b affords (E)- and (Z)-1-bromo-2-p-chlorophenyl-1-phenyl-2-p-chlorophenylsulfonylethylenes (6a and 6b), which upon reaction with the p-chlorobenzenethiol gave (E)- and (Z)-1-p-chlorophenyl-1-p-chlorophenylsulfonyl-2-phenyl-2-p-chlorophenylthioethylenes (7a and 7b). Oxidation of 7a and 7b yielded (E)- and (Z)-1,2-bis(p-chlorophenylsulfonyl)-2-phenyl-1-p-chlorophenylethylenes (8a and 8b). The final products, 8a and 8b, were also synthesized from a mixture of diastereomers, (E)- and (Z)-2-p-chlorophenyl-1-phenyl-1-p-chlorophenylthioethylenes (3 and 4), yielding the intermediates 9a and 9b, 10a and 10b, and 11a and 11b. The configurations of these compounds were established by elemental analysis, IR, 1 H NMR, and mass spectra, and by their preparation from the corresponding phenylketones and p-chlorophenylphenylacetylene. All these new compounds exhibited pronounced in vitro antibacterial and antifungal activities. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. GRAPHICAL ABSTRACT
doi_str_mv 10.1080/10426507.2010.530629
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Narayana</creatorcontrib><title>Synthesis and Biological Evaluation of Diastereomeric (E and Z) Sulfides, Sulfones, Sulfide-Sulfones, and Disulfones</title><title>Phosphorus, sulfur, and silicon and the related elements</title><description>The addition of p-chlorobenzenethiol to benzyl p-chlorophenylketone resulted in the formation of a mixture of diastereomers (E)- and (Z)-1-p-chlorophenyl-2-phenyl-1-p-chlorophenylthioethylene (1 and 2). These compounds, upon reaction with bromine in acetic acid, yielded a mixture of (E)- and (Z)-1-bromo-2-p-chlorophenyl-1-phenyl-2-p-chlorophenylthioethylenes (5a and 5b). Oxidation of 5a and 5b affords (E)- and (Z)-1-bromo-2-p-chlorophenyl-1-phenyl-2-p-chlorophenylsulfonylethylenes (6a and 6b), which upon reaction with the p-chlorobenzenethiol gave (E)- and (Z)-1-p-chlorophenyl-1-p-chlorophenylsulfonyl-2-phenyl-2-p-chlorophenylthioethylenes (7a and 7b). 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source Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Science and Technology Collection (Reading list)
subjects (E)- and (Z)-isomers, sulfide-sulfones
Antimicrobial activity
disulfones
sulfides
sulfones
title Synthesis and Biological Evaluation of Diastereomeric (E and Z) Sulfides, Sulfones, Sulfide-Sulfones, and Disulfones
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