Highly enantioselective aldol reaction of acetone with β,γ- unsaturated α-keto esters promoted by simple chiral primary-tertiary diamine catalysts

Organic and Biomolecular Chemistry

Volumn 9, Issue 13, 2011, Pages 4774-4777

  Peng, Lin ^a,b   Wang, Liang Liang ^a,b   Bai, Jian Fei ^a,b   Jia, Li Na ^a,b   Guo, Yun Long ^a,b   Luo, Xi Ya ^a,b   Wang, Fei Ying ^a   Xu, Xiao Ying ^a   Wang, Li Xin ^a  

^a CHENGDU INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL REACTIONS; ENANTIOSELECTIVE; KETO ESTER;

ACETONE; CATALYSTS; ENANTIOSELECTIVITY; ESTERIFICATION; ESTERS;

CONDENSATION REACTIONS;

3-HYDROXYBUTANAL; ACETONE; ALDEHYDE; ALDOL; DIAMINE; ESTER;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM;

ACETONE; ALDEHYDES; CATALYSIS; DIAMINES; ESTERS; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 79959791655     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob05607g     Document Type: Article

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