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Volumn 8, Issue 10, 2010, Pages 2320-2322
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Chiral 1-phenylethylamine-derived phosphine-phosphoramidite ligands for highly enantioselective Rh-catalyzed hydrogenation of β-(acylamino) acrylates: Significant effect of substituents on 3,3′-positions of binaphthyl moiety
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Author keywords
[No Author keywords available]
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Indexed keywords
1-PHENYLETHYLAMINE;
ASYMMETRIC HYDROGENATION;
BINAPHTHYL MOIETY;
CHIRAL PHOSPHINE;
ENANTIOSELECTIVE;
PHOSPHORAMIDITE LIGANDS;
ENANTIOSELECTIVITY;
HYDROGENATION;
PHOSPHORUS COMPOUNDS;
RHODIUM;
SALTS;
LIGANDS;
ACRYLIC ACID DERIVATIVE;
LIGAND;
NAPHTHALENE;
NAPHTHALENE DERIVATIVE;
ORGANOPHOSPHORUS COMPOUND;
PHENETHYLAMINE DERIVATIVE;
PHOSPHINE DERIVATIVE;
PHOSPHORAMIDOUS ACID;
RHODIUM;
ARTICLE;
CATALYSIS;
CHEMISTRY;
ENZYME SPECIFICITY;
HYDROGENATION;
STEREOISOMERISM;
ACRYLATES;
CATALYSIS;
HYDROGENATION;
LIGANDS;
NAPHTHALENES;
ORGANOPHOSPHORUS COMPOUNDS;
PHENETHYLAMINES;
PHOSPHINES;
RHODIUM;
STEREOISOMERISM;
SUBSTRATE SPECIFICITY;
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EID: 77952393132
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c000268b Document Type: Article |
Times cited : (15)
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References (37)
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