Direct vinylogous aldol reaction triggered by tetrabutylammonium fluoride: A highly regioselective and diastereoselective addition of cyclic β-haloenals to aromatic aldehydes

Synlett

Volumn , Issue 3, 2012, Pages 468-472

  Zhang, Jingli ^a   Gu, Lianghu ^a   Gong, Yuefa ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

cyclic haloenals; direct vinylogous aldol reaction; homoallylic alcohols; regio and diastereoselectivity; TBAF

Indexed keywords

ALDEHYDE; BENZALDEHYDE; CYCLIC DIENOLATE; HETEROAROMATIC 2 FURALADEHYDE; NAPTHYLALDEHYDE; REAGENT; TETRABUTYLAMMONIUM FLUORIDE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CHEMICAL INTERACTION; DIRECT VINYLOGOUS ALDOL REACTION; ELECTROPHILICITY; NUCLEOPHILICITY; PROTON TRANSPORT; REACTION OPTIMIZATION; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 84862825931     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290313     Document Type: Article

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