4.4 Article

Diastereoselective Henry reactions of N,N-dibenzyl α-amino aldehydes with nitromethane catalyzed by enantiopure guanidines

Journal

TETRAHEDRON LETTERS
Volume 43, Issue 51, Pages 9401-9403

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(02)02332-8

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Several enantiopure guanidines are studied as the catalysts of Henry reactions of N,N-dibenzyl alpha-amino aldehydes with nitromethane. Good diastereoselectivity is observed in the reactions of L-valine or L-isoleucine derived aldehydes catalyzed by a (R)-1-(1-naphthyl)ethylamine derived guanidine. (C) 2002 Elsevier Science Ltd. All rights reserved.

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