Paper

Chemoenzymatic synthesis of (3 S,4 S)- and (3 R,4 R)-3-methoxy-4-methylaminopyrrolidine

Published Oct 18, 2004 · A. Kamal, Ahmad Ali Shaik, Mahendra Sandbhor

Tetrahedron Letters

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Abstract

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Study Snapshot

Chemoenzymatic enantioselective synthesis of (3S,4S)-3-methoxy-4-methylaminopyrrolidine, a key intermediate for the new quinolone antitumor compound AG-7352, is a feasible method for preparing key intermediates

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Chemoenzymatic synthesis of (3 S,4 S)- and (3 R,4 R)-3-methoxy-4-methylaminopyrrolidine

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