Efficient asymmetric Michael reaction of 2-oxindole-3-carboxylate esters with maleimides catalyzed by cinchonidine

Tetrahedron

Volumn 70, Issue 21, 2014, Pages 3478-3484

  Zhou, Jing ^a,b   Jia, Li Na ^a,b   Peng, Lin ^a   Wang, Qi Lin ^a,b   Tian, Fang ^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

2 Oxindole 3 carboxylate esters; Cinchonidine; Maleimides; Michael reaction

Indexed keywords

2 OXINDOLE 3 CARBOXYLATE ESTER DERIVATIVE; CINCHONIDINE; ESTER DERIVATIVE; MALEIMIDE DERIVATIVE; OXINDOLE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CRYSTAL STRUCTURE; ENANTIOSELECTIVITY; MICHAEL ADDITION; PRIORITY JOURNAL;

EID: 84899463305     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.03.065     Document Type: Article

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