A highly enantioselective one-pot synthesis of spirolactones by an organocatalyzed michael addition/cyclization sequence

Angewandte Chemie - International Edition

Volumn 50, Issue 40, 2011, Pages 9382-9385

  Sternativo, Silvia ^a   Calandriello, Antonella ^a   Costantino, Ferdinando ^a   Testaferri, Lorenzo ^a   Tiecco, Marcello ^a   Marini, Francesca ^a  

^a UNIVERSITY OF PERUGIA   (Italy)

Author keywords

cyclization; nucleophilic addition; organocatalysis; selenium; spiro compounds

Indexed keywords

ENANTIOSELECTIVE; FUNCTIONALIZED; HIGH YIELD; IN-CONTROL; MICHAEL ADDITIONS; MILD REACTION CONDITIONS; NUCLEOPHILIC ADDITIONS; ONE-POT PROCEDURES; ONE-POT SYNTHESIS; ORGANOCATALYSIS; ORGANOCATALYTIC; SELENONES; SPIRO COMPOUNDS;

ADDITION REACTIONS; ENANTIOSELECTIVITY; REACTION KINETICS; SELENIUM; SYNTHESIS (CHEMICAL);

CYCLIZATION;

LACTONE; SELENIUM; SPIRO COMPOUND;

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

CATALYSIS; CHEMISTRY TECHNIQUES, SYNTHETIC; CYCLIZATION; LACTONES; MOLECULAR STRUCTURE; SELENIUM; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 80053160823     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201104819     Document Type: Article

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