Paper

Stereoselective synthesis of (2R, 3R, 4R)-3-hydroxy-2,4,6-trimethylheptanoic acid and determination of the absolute stereochemistry of the natural product from callipeltin A

Published Jul 5, 2002 · DOI · A. Zampella, M. V. D’Auria

Tetrahedron-asymmetry

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Abstract

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Study Snapshot

The revised stereostructure of 3-hydroxy-2,4,6-trimethylheptanoic acid, found in callipeltin A, was confirmed by enantioselective synthesis.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Stereoselective synthesis of (2R, 3R, 4R)-3-hydroxy-2,4,6-trimethylheptanoic acid and determination of the absolute stereochemistry of the natural product from callipeltin A

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