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Direct Diastereo- and Enantioselective Vinylogous Michael Additions of Linear Enones.
Guo, Qunsheng; Fraboni, Americo J; Brenner-Moyer, Stacey E.
Afiliação
  • Guo Q; Department of Chemistry, Rutgers University , 73 Warren Street, Newark, New Jersey 07102, United States.
  • Fraboni AJ; Department of Chemistry, Rutgers University , 73 Warren Street, Newark, New Jersey 07102, United States.
  • Brenner-Moyer SE; Department of Chemistry, Rutgers University , 73 Warren Street, Newark, New Jersey 07102, United States.
Org Lett ; 18(11): 2628-31, 2016 06 03.
Article em En | MEDLINE | ID: mdl-27186662
ABSTRACT
A direct vinylogous Michael addition using linear vinylogous Michael donors has been developed. Notably, even γ-substituted Michael donors cleanly afforded γ-alkylated products in high yield and ee by this method. Moreover, control experiments revealed that, for these and related linear vinylogous Michael donors, the size of the Michael acceptor strongly influences whether α- or γ-alkylation occurs, not simply blocking effects of cocatalysts as suggested previously.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article