Applications of Baylis–Hillman chemistry: enantioselective synthesis of (−)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy

doi:10.1016/S0040-4020(01)00786-4

Paper

Applications of Baylis–Hillman chemistry: enantioselective synthesis of (−)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy

Published Sep 17, 2001 · D. Basavaiah, N. Kumaragurubaran, D. Sharada

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Q3 SJR score

35

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Abstract

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Study Snapshot

Baylis-Hillman chemistry allows for enantioselective synthesis of ()-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates in 25- 40% enantiomeric purity.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Applications of Baylis–Hillman chemistry: enantioselective synthesis of (−)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy

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