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Volumn 57, Issue 11, 2001, Pages 2155-2170

Copper(I) mediated highly diastereoselective conjugate addition of Grignard reagents to functionalised cycloalkenols: A general and efficient route for the stereoselective synthesis of 5- and 6-membered ring trisubstituted cycloalkanols

(7) Dambrin, Valéry a Villiéras, Monique a Janvier, Pascal a Toupet, Loïc b Amri, Hassen c Lebreton, Jacques a Villiéras, Jean a

a Centre National de la Recherche Scientifique (France)

b CNRS (France)

c FACULTÉ DES SCIENCES DE TUNIS (Tunisia)

Author keywords

Conjugate addition; Diastereoselectivity; Grignard reagents; Micha l addition; Organocuprates; SN2 ; elimination

Indexed keywords

2 SILYLOXYCYCLOHEXENE CARBOXYLATE; 2 SILYLOXYCYCLOPENTENE CARBOXYLATE; ALCOHOL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; COPPER; COPPER DERIVATIVE; CYCLOALKANOL; CYCLOALKENOL; CYCLOHEXANOL; CYCLOPENTANOL; MAGNESIUM CUPRATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CONJUGATION; CYCLIZATION; ISOMERISM; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0035835952 PISSN: 00404020 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4020(01)00044-8 Document Type: Article

Times cited : (26)

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