A novel asymmetric organocatalytic Michael-aldol-dehydration domino reaction for the construction of spirocyclic benzofuranones

Tetrahedron

Volumn 69, Issue 44, 2013, Pages 9303-9308

  Qi, Liang Wen ^a,b   Wang, Liang Liang ^a,b   Peng, Lin ^a,b   Jia, Li Na ^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

Asymmetric catalysis; Benzofuranone; Domino reaction; Organocatalysis; Spirocyclic compound

Indexed keywords

3 (1 HYDROXYETHYLIDENE)BENZOFURAN 2(3H) ONE; FURANONE DERIVATIVE; SPIRO COMPOUND; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; ASYMMETRIC CATALYSIS; CHIRALITY; CINCHONA; ELECTROPHILICITY; ENANTIOSELECTIVITY; MICHAEL ADDITION; NUCLEOPHILICITY; PRIORITY JOURNAL; STEREOCHEMISTRY; STEREOSPECIFICITY;

EID: 84884405952     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.08.030     Document Type: Article

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