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Angewandte Chemie - International Edition

Volumn 50, Issue 39, 2011, Pages 9124-9127

Enantioselective Michael/cyclization reaction sequence: Scaffold-inspired synthesis of spirooxindoles with multiple stereocenters

(6) Cao, Yiming a Jiang, Xianxing a Liu, Luping a Shen, Fangfang a Zhang, Futing a Wang, Rui a,b

a LANZHOU UNIVERSITY (China)

b HONG KONG POLYTECHNIC UNIVERSITY (Hong Kong)

Author keywords

asymmetric synthesis; heterocycles; Michael addition; organocatalysis; synthetic methods

Indexed keywords

ASYMMETRIC SYNTHESIS; HETEROCYCLES; MICHAEL ADDITIONS; ORGANOCATALYSIS; SYNTHETIC METHODS;

ADDITION REACTIONS; ENANTIOSELECTIVITY; REACTION KINETICS; SCAFFOLDS;

SYNTHESIS (CHEMICAL);

IMIDE; INDOLE DERIVATIVE; MANNICH BASE; OXINDOLE; SPIRO COMPOUND;

ARTICLE; CATALYSIS; CHEMISTRY; CYCLIZATION; STEREOISOMERISM;

CATALYSIS; CYCLIZATION; IMIDES; INDOLES; MANNICH BASES; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 80052833054 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201104216 Document Type: Article

Times cited : (255)

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