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Merck

Organocatalytic enantioselective indole alkylations of alpha,beta-unsaturated ketones.

Organic & biomolecular chemistry (2007-02-23)
Wei Chen, Wei Du, Lei Yue, Rui Li, Yong Wu, Li-Sheng Ding, Ying-Chun Chen
RESUMO

The C3-selective enantioselective Michael-type Friedel-Crafts alkylations of indoles with nonchelating alpha,beta-unsaturated alkyl ketones, catalysed by a chiral primary amine derived from natural cinchonine, were investigated. The reactions, in the presence of 30 mol% catalyst, were smoothly conducted at 0 to -20 degrees C. Moderate to good ee (47-89%) has been achieved.

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Sigma-Aldrich
(+)-Cinchonine, 85%
Sigma-Aldrich
Cinchonine, crystallized, ≥98.0% (NT)