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Rhodium-catalyzed enantioselective addition of boronic acids to N-benzylnicotinate salts.

Journal of the American Chemical Society (2011-02-12)
Nadeau Christian, Sara Aly, Kevin Belyk
ABSTRAKT

The highly enantioselective catalytic asymmetric addition of aryl and alkenylboronic acids to N-benzylnicotinate salt 1 is described. The dihydropyridine 2 reaction products can be converted to synthetically useful piperidines. Application of the methodology to the preparation of enantioenriched quaternary chiral centers is also discussed.

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Sigma-Aldrich
Benzyl nicotinate, ≥98.0% (GC)