Paper
Chemoenzymatic synthesis of (3R,4S)- and (3S,4R)-3-methoxy-4-methylaminopyrrolidine
Published Nov 6, 2006 · A. Kamal, Ahmad Ali Shaik, Mahendra Sandbhor
Tetrahedron-asymmetry
UNKNOWN SJR score
14
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
This study presents an efficient and convenient enantioselective synthesis of (3R,4S)-3-methoxy-4-methylaminopyrrolidine using a lipase-mediated resolution protocol.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
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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
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