Reaction of trifluoromethyl-containing enones with thiophenol derivatives

doi:10.1002/CHIN.200012059

Paper

DOI: 10.1002/CHIN.200012059

Reaction of trifluoromethyl-containing enones with thiophenol derivatives

Published May 1, 1999 · V. Nenajdenko, A. Sanin, A. Churakov

Chemistry of Heterocyclic Compounds

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Abstract

The reaction of trifluoromethyl-containing enones with thiophenol derivatives has been studied. Reactions with 4-methylthiophenol proceed with the formation of either ketosulfides or a pyran derivative. Reactions of trifluoromethyl-containing enones with 2-mercaptobenzaldehyde lead to 3-trifluoroacetyl-substituted 2H-thiochromenes.

Study Snapshot

Trifluoromethyl-containing enones can form ketosulfides or pyran derivatives when reacting with 4-methylthiophenol, and 3-trifluoroacetyl-substituted 2H-thiochromenes when reacting with 2-mercaptobenzaldehy

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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