Enantioselective iridium-catalyzed vinylogous reformatsky-aldol reaction from the alcohol oxidation level: Linear regioselectivity by way of carbon-bound enolates

Angewandte Chemie - International Edition

Volumn 50, Issue 15, 2011, Pages 3493-3496

  Hassan, Abbas ^a   Zbieg, Jason R ^a   Krische, Michael J ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

Author keywords

aldol reaction; allylation; homogeneous catalysis; iridium; transfer hydrogenation

Indexed keywords

ALCOHOL OXIDATION; ALDOL REACTIONS; CHIRAL ALCOHOLS; DIASTEREO-SELECTIVITY; ENANTIOSELECTIVE; ENOLATES; HOMOGENEOUS CATALYSIS; TRANSFER HYDROGENATION;

ALLYLATION; CATALYSIS; HYDROGENATION; IRIDIUM; OXIDATION; REACTION KINETICS; REGIOSELECTIVITY;

CONDENSATION REACTIONS;

3-HYDROXYBUTANAL; ALCOHOL DERIVATIVE; ALDEHYDE; ALDOL; IRIDIUM; VINYL DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM;

ALCOHOLS; ALDEHYDES; CATALYSIS; IRIDIUM; MOLECULAR STRUCTURE; STEREOISOMERISM; VINYL COMPOUNDS;

EID: 79953236209     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201100646     Document Type: Article

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