Enantioselective synthesis of endocyclic β-amino acids with two contiguous stereocenters via hydrogenation of 3-alkoxycarbonyl-2-substituted quinolines

Synthesis (Germany)

Volumn 45, Issue 23, 2013, Pages 3239-3244

  Chen, Zhang Pei ^a   Ye, Zhi Shi ^a   Chen, Mu Wang ^a   Zhou, Yong Gui ^a  

^a DALIAN INSTITUTE OF CHEMICAL PHYSICS   (China)

Author keywords

amino acids; asymmetric hydrogenation; functionalized quinolines; iridium

Indexed keywords

ASYMMETRIC HYDROGENATION; CONTIGUOUS STEREOCENTERS; ENANTIOPURE; ENANTIOSELECTIVE; ENANTIOSELECTIVE SYNTHESIS; FUNCTIONALIZED; QUINOLINE DERIVATIVE;

ENANTIOSELECTIVITY; HYDROGENATION; IRIDIUM; IRIDIUM COMPOUNDS;

AMINO ACIDS;

AMINO ACID; BUTYL 2 METHYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; EPOXIDE; ETHYL 2 METHYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; ETHYL 2 PHENYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; ETHYL 2 PROPYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; IRIDIUM; ISOPROPYL 2 METHYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; METHYL 2 ETHYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; METHYL 2 ISOPROPYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; METHYL 2 ISOPROPYL 6 METHOXY 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; METHYL 2 PENTYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; METHYL 6 CHLORO 2 ISOPROPYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; METHYL 6 FLUORO 2 ISOPROPYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; PROPYL 2 METHYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; QUINOLINE; TERT BUTYL 2 METHYL 1,2,3,4 TETRAHYDROQUINOLINE 3 CARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHIRALITY; CONFORMATIONAL TRANSITION; CYCLOADDITION; ENANTIOSELECTIVITY; HYDROGENATION; STEREOCHEMISTRY;

EID: 84888133773     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0033-1339849     Document Type: Article

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