1,n-Glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1,3-polyols

Angewandte Chemie - International Edition

Volumn 48, Issue 27, 2009, Pages 5018-5021

  Lu, Yu ^a   Kim, In Su ^a   Hassan, Abbas ^a   Del Valle, David J ^a   Krische, Michael J ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

Author keywords

Allylatlon; Diols; Enantioselectivity; Iridium; Transfer hydrogenation

Indexed keywords

ALCOHOL OXIDATION; ALLYLATLON; ASYMMETRIC ALLYLATION; CARBONYL ALLYLATION; DIALDEHYDES; DIOLS; ENANTIOSELECTIVE; POLYOLS; PROPANEDIOLS; STEREOCONTROL; SYNTHETIC EQUIVALENTS; TRANSFER HYDROGENATION; TRANSFER HYDROGENATIONS;

ALDEHYDES; CARBONYLATION; ELECTRON TRANSITIONS; ENANTIOSELECTIVITY; GLYCOLS; HYDROGENATION;

IRIDIUM;

ALDEHYDE; IRIDIUM; POLYMER; POLYOL;

CATALYSIS; CHEMISTRY; HYDROGENATION; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

ALDEHYDES; CATALYSIS; HYDROGENATION; IRIDIUM; OXIDATION-REDUCTION; POLYMERS; STEREOISOMERISM;

EID: 70349786246     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200901648     Document Type: Article

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