π-allyl palladium complexes as efficient and powerful alternative for nucleophilic substitution on bicyclo[3.1.0]hexane sulfonates: Regio-, chemo- and stereoselectivity

Synlett

Volumn , Issue 9, 2006, Pages 1407-1409

  Lecornué, Frédéric ^b   Charnay Pouget, Florence ^a   Ollivier, Jean ^a  

^a UNIVERSITÉ PARIS SUD   (France)

^b UNIVERSITÉ DE POITIERS   (France)

Author keywords

Chemoselectivity; Complexes; Nucleophilic additions; Palladium; Regioselectivity; Ring opening

Indexed keywords

6 (2' CHLOROETHYL)BICYCLO[3.1.0]HEXANE 6 OL; BICYCLO[3.1.0]HEXANE SULFONATE; CYCLOPROPANE; CYCLOPROPYLIDEN BICYCLO[3.1.0]HEXANE SULFONATE; PALLADIUM COMPLEX; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLOPROPANATION; ENANTIOSELECTIVITY; RING OPENING; STEREOCHEMISTRY; SUBSTITUTION REACTION; SYNTHESIS;

EID: 33745369481     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-939716     Document Type: Article

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