Dynamic kinetic resolution allows a highly enantioselective synthesis of cis-α-aminocycloalkanols by ruthenium-catalyzed asymmetric hydrogenation

Angewandte Chemie - International Edition

Volumn 46, Issue 39, 2007, Pages 7506-7508

  Liu, Sheng ^a   Xie, Jian Hua ^a   Wang, Li Xin ^a   Zhou, Qi Lin ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

Amino alcohols; Asymmetric catalysis; Diamines; Hydrogenation; Ruthenium

Indexed keywords

AMINES; CATALYSIS; ENANTIOSELECTIVITY; HYDROGENATION; REACTION KINETICS; RUTHENIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

AMINO ALCOHOLS; ASYMMETRIC CATALYSIS; DIAMINES;

ALCOHOLS;

3,4 DICHLORO N METHYL N [2 (1 PYRROLIDINYL)CYCLOHEXYL]BENZENEACETAMIDE; AMIDE; CYCLOALKANE DERIVATIVE; RUTHENIUM;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; HYDROGENATION; KINETICS; STEREOISOMERISM; SYNTHESIS;

3,4-DICHLORO-N-METHYL-N-(2-(1-PYRROLIDINYL)-CYCLOHEXYL)-BENZENEACETAMIDE, (TRANS)-ISOMER; AMIDES; CATALYSIS; CYCLOPARAFFINS; HYDROGENATION; KINETICS; MOLECULAR STRUCTURE; RUTHENIUM; STEREOISOMERISM;

EID: 35048869670     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200702491     Document Type: Article

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