An organocatalytic [3+2] cyclisation strategy for the highly enantioselective synthesis of spirooxindoles

Chemistry - A European Journal

Volumn 16, Issue 42, 2010, Pages 12541-12544

  Voituriez, Arnaud ^a   Pinto, Nathalie ^a   Neel, Mathilde ^a   Retailleau, Pascal ^a   Marinetti, Angela ^a  

^a CNRS   (France)

Author keywords

cyclization; organocatalysis; oxindoles; phosphanes; spiro compounds

Indexed keywords

ALLENES; ANNULATION REACTIONS; ASYMMETRIC INDUCTION; ASYMMETRIC VARIANTS; CHIRAL CATALYST; CYCLISATIONS; ENANTIOSELECTIVE SYNTHESIS; ORGANOCATALYSIS; ORGANOCATALYTIC; OXINDOLES; PHOSPHANES; SPIRO COMPOUNDS;

CATALYSIS; COMPLEXATION; HYDROCARBONS; PHOSPHORUS COMPOUNDS; RATE CONSTANTS; REACTION KINETICS;

CYCLIZATION;

ALKADIENE; INDOLE DERIVATIVE; PHOSPHINE DERIVATIVE; SPIRO COMPOUND;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; SYNTHESIS;

ALKADIENES; CATALYSIS; CYCLIZATION; INDOLES; MOLECULAR STRUCTURE; PHOSPHINES; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 78249241499     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001791     Document Type: Article

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