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National Institutes of Health
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Chemoenzymatic synthesis of all four diastereomers of 2,6-disubstituted piperidines through stereoselective monoamination of 1,5-diketones.
R. C. Simon
Corpus ID: 32311523
The regioselectivity of various enantiocomplementary ω-transaminases was evaluated for the stereoselective monoamination of…
A new route to trans-2,6-disubstituted piperidine-related alkaloids using a novel C2-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester.
Organic & biomolecular chemistry
Corpus ID: 12543889
A novel C2-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester 1 was prepared by the double asymmetric allylboration of…
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