Paper

Nucleophilic reactions with α-trifluoromethyl imine and N,O-disubstituted aminal: synthesis of β-trifluoromethyl β-anilino esters

Published Sep 28, 2001 · DOI · Y. Gong, Katsuya Kato

Journal of Fluorine Chemistry

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Abstract

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Study Snapshot

The Reformatsky reaction with -trifluoromethyl imine and N,O-disubstituted aminal yields ethyl 4,4,4-trifluoro-3-(N-4-methoxyphenyl)amino-2-alkylbutyrate and

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Nucleophilic reactions with α-trifluoromethyl imine and N,O-disubstituted aminal: synthesis of β-trifluoromethyl β-anilino esters

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