Catalytic asymmetric michael addition/cyclization of isothiocyanato oxindoles: Highly efficient and versatile approach for the synthesis of 3,2′-pyrrolidinyl mono- and bi-spirooxindole frameworks

Chemistry - A European Journal

Volumn 19, Issue 4, 2013, Pages 1184-1188

  Cao, Yi Ming ^a   Shen, Fang Fang ^a   Zhang, Fu Ting ^a   Wang, Rui ^a,b  

^a LANZHOU UNIVERSITY   (China)

^b HONG KONG POLYTECHNIC UNIVERSITY   (Hong Kong)

Author keywords

asymmetric synthesis; heterocycles; organocatalysis; oxindoles; spiro compounds; synthetic methods

Indexed keywords

ASYMMETRIC SYNTHESIS; HETEROCYCLES; ORGANOCATALYSIS; OXINDOLES; SPIRO COMPOUNDS; SYNTHETIC METHODS;

CHEMISTRY; SYNTHESIS (CHEMICAL);

REACTION KINETICS;

INDOLE DERIVATIVE; OXINDOLE; SPIRO COMPOUND;

ARTICLE; CATALYSIS; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; CYCLIZATION; INDOLES; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84872454361     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201204114     Document Type: Article

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