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Copper-Catalyzed Asymmetric Conjugate Additions of Bis(pinacolato)diboron and Dimethylzinc to Acyl- N-methylimidazole Michael Acceptors: A Highly Stereoselective Unified Strategy for 1,3,5,... n (OH, Me) Motif Synthesis.
Lauberteaux, Jimmy; Crévisy, Christophe; Baslé, Olivier; de Figueiredo, Renata Marcia; Mauduit, Marc; Campagne, Jean-Marc.
Afiliación
  • Lauberteaux J; Institut Charles Gerhardt Montpellier , UMR 5253 CNRS-UM-ENSCM, Ecole Nationale Supérieure de Chimie, Avenue Emile Jeanbrau , Montpellier 34296 Cedex 6 , France.
  • Crévisy C; Univ Rennes, Ecole Nationale Supérieure de Chimie de Rennes , CNRS, ISCR UMR 6226, F-35000 Rennes , France.
  • Baslé O; Univ Rennes, Ecole Nationale Supérieure de Chimie de Rennes , CNRS, ISCR UMR 6226, F-35000 Rennes , France.
  • de Figueiredo RM; Institut Charles Gerhardt Montpellier , UMR 5253 CNRS-UM-ENSCM, Ecole Nationale Supérieure de Chimie, Avenue Emile Jeanbrau , Montpellier 34296 Cedex 6 , France.
  • Mauduit M; Univ Rennes, Ecole Nationale Supérieure de Chimie de Rennes , CNRS, ISCR UMR 6226, F-35000 Rennes , France.
  • Campagne JM; Institut Charles Gerhardt Montpellier , UMR 5253 CNRS-UM-ENSCM, Ecole Nationale Supérieure de Chimie, Avenue Emile Jeanbrau , Montpellier 34296 Cedex 6 , France.
Org Lett ; 21(6): 1872-1876, 2019 03 15.
Article en En | MEDLINE | ID: mdl-30802071
A unified strategy for the construction of prevalent 1,3,5,... n (OH, Me) motifs based on consecutive copper-catalyzed asymmetric conjugate borylation (ACB) and methylation (ACA) reactions involving α,ß-unsaturated 2-acyl- N-methylimidazoles is described. Good yields and high diastereoselectivities have been obtained in ACA and ACB reactions for both matched and mismatched pairs as illustrated in the synthesis of syn/ anti and anti/ anti (Me, OTBS, Me) and (OH, OTBS, Me) motifs.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos