Synthesis of 3-fluoro-2-substituted amino-5,12-dihydro-5-oxobenzoxazolo[3,2-a]quinoline-6-carboxylic acids employing the tandem double ring closure reaction of N-acetyl-N-(2-hydroxyphenyl)anthranilic acid as the key step

doi:10.1016/0040-4020(95)00809-M

Paper

Synthesis of 3-fluoro-2-substituted amino-5,12-dihydro-5-oxobenzoxazolo[3,2-a]quinoline-6-carboxylic acids employing the tandem double ring closure reaction of N-acetyl-N-(2-hydroxyphenyl)anthranilic acid as the key step

Published Nov 13, 1995 · Sang J. Chung, D. H. Kim

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14

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Abstract

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Study Snapshot

The tandem double ring closure reaction of N-acetyl-N-(2-hydroxyphenyl)anthranilic acid effectively synthesized 3-fluoro-2-substituted amino-5,12-dihydro-5-oxobenzoxazolo[3,2-a]

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Synthesis of 3-fluoro-2-substituted amino-5,12-dihydro-5-oxobenzoxazolo[3,2-a]quinoline-6-carboxylic acids employing the tandem double ring closure reaction of N-acetyl-N-(2-hydroxyphenyl)anthranilic acid as the key step

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