A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric mannich reactions of N-boc-protected imines

Angewandte Chemie - International Edition

Volumn 48, Issue 10, 2009, Pages 1838-1840

  Kano, Taichi ^a   Yamaguchi, Yukako ^a   Maruoka, Keiji ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

Asymmetric catalysis; Diastereoselectivity; Enantioselectivity; Mannich reaction; Organocatalysis

Indexed keywords

ALDEHYDES; AMINATION; AMINES; ELECTRON TRANSITIONS; ENANTIOSELECTIVITY; NITROGEN COMPOUNDS; RATE CONSTANTS; REACTION KINETICS; STEREOSELECTIVITY; SULFUR COMPOUNDS;

ALDOL REACTIONS; ASYMMETRIC CATALYSIS; DIASTEREOSELECTIVITY; GOOD YIELDS; MANNICH REACTION; NUCLEOPHILICITY; ORGANOCATALYSIS; ORGANOCATALYST; SIDE REACTIONS;

CATALYSIS;

ALDEHYDE; IMINE; MANNICH BASE; NITROGEN; SULFONAMIDE;

ARTICLE; CATALYSIS; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ALDEHYDES; CATALYSIS; IMINES; MANNICH BASES; NITROGEN; STEREOISOMERISM; SULFONAMIDES;

EID: 61349122678     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200805628     Document Type: Article

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