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Angewandte Chemie - International Edition

Volumn 52, Issue 18, 2013, Pages 4925-4928

Ruthenium-catalyzed asymmetric transfer hydrogenation of 1-aryl-substituted dihydroisoquinolines: Access to valuable chiral 1-aryl-tetrahydroisoquinoline scaffolds

(5) Wu, Zi a Perez, Marc a Scalone, Michelangelo b Ayad, Tahar a Ratovelomanana Vidal, Virginie a

a PSL RESEARCH UNIVERSITY (France)

b F HOFFMANN LA ROCHE LTD (Switzerland)

Author keywords

asymmetric catalysis; enantioselectivity; hydrogen transfer; isoquinolines; ruthenium

Indexed keywords

ASYMMETRIC CATALYSIS; ASYMMETRIC TRANSFER HYDROGENATION; DIHYDROISOQUINOLINES; ENANTIOSELECTIVE; HIGH YIELD; HYDROGEN TRANSFER; ISOQUINOLINES; TRANSFER HYDROGENATIONS;

AROMATIC COMPOUNDS; ENANTIOSELECTIVITY; HYDROGENATION; RUTHENIUM; SCAFFOLDS;

CATALYSIS;

AMPA RECEPTOR; ANTICONVULSIVE AGENT; G 1617; ISOQUINOLINE DERIVATIVE; RUTHENIUM; TETRAHYDROISOQUINOLINE DERIVATIVE;

ARTICLE; CATALYSIS; CHEMISTRY; DRUG ANTAGONISM; HYDROGENATION; METABOLISM; STEREOISOMERISM; SYNTHESIS;

ANTICONVULSANTS; CATALYSIS; HYDROGENATION; ISOQUINOLINES; RECEPTORS, AMPA; RUTHENIUM; STEREOISOMERISM; TETRAHYDROISOQUINOLINES;

EID: 84876560042 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201301134 Document Type: Article

Times cited : (68)

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