4.8 Article

An enantioselective chiral bronsted acid catalyzed imino-azaenamine reaction

Journal

ORGANIC LETTERS
Volume 9, Issue 6, Pages 1065-1068

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol063112p

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The enantioselective Bronsted acid catalyzed addition of methyleneaminopyrrolidine to N-Boc imines has been achieved in the presence of chiral phosphoric acids derived from 3,3'-di(phenanthryl)-H8-BINOL. The corresponding aminohydrazones have been isolated in good yields with enantiomeric excesses up to 90%.

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