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Volumn 13, Issue 1, 2002, Pages 37-42

Enantioselective catalysis. Part 143: Astonishingly high enantioselectivity in the transfer hydrogenation of acetophenone with 2-propanol using Ru complexes of the Schiff base derived from (S)-2-amino-2′-hydroxy-1,1′-binaphthyl (NOBIN) and 2-pyridinecarbaldehyde

(3) Brunner, Henri a Henning, Frauke a Weber, Matthias a

a UNIVERSITY OF REGENSBURG (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

1 PHENYLETHANOL; 2 AMINO 2' HYDROXYL 1,1' BINAPHTHYL; 2 PROPANOL; 2 PYRIDINECARBALDEHYDE; ACETOPHENONE; ALDEHYDE DERIVATIVE; IMINE; LIGAND; NAPHTHYL GROUP; RUTHENIUM; SCHIFF BASE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOSELECTIVITY; HYDROGENATION; METHYLATION; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; PROTON TRANSPORT; QUANTITATIVE ANALYSIS; REDUCTION; SYNTHESIS; TEMPERATURE;

EID: 0037070075 PISSN: 09574166 EISSN: None Source Type: Journal
DOI: 10.1016/S0957-4166(02)00029-0 Document Type: Article

Times cited : (65)

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