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Nickel-Catalyzed Synthesis of Stereochemically Defined Enamides via Bi- and Tricomponent Coupling Reaction.
Liu, Y; De Nisi, A; Cerveri, A; Monari, M; Bandini, M.
Afiliação
  • Liu Y; Department of Chemistry "G. Ciamician", Alma Mater Studiorum, University of Bologna , via Selmi 2, 40126 Bologna, Italy.
  • De Nisi A; Department of Chemistry "G. Ciamician", Alma Mater Studiorum, University of Bologna , via Selmi 2, 40126 Bologna, Italy.
  • Cerveri A; Department of Chemistry "G. Ciamician", Alma Mater Studiorum, University of Bologna , via Selmi 2, 40126 Bologna, Italy.
  • Monari M; Department of Chemistry "G. Ciamician", Alma Mater Studiorum, University of Bologna , via Selmi 2, 40126 Bologna, Italy.
  • Bandini M; Department of Chemistry "G. Ciamician", Alma Mater Studiorum, University of Bologna , via Selmi 2, 40126 Bologna, Italy.
Org Lett ; 19(19): 5034-5037, 2017 10 06.
Article em En | MEDLINE | ID: mdl-28901140
ABSTRACT
The stereoselective synthesis of (E)-trisubstituted tertiary enamides is documented via site-selective Ni-catalyzed ß-arylation of allenamides with boronic acids in high yields (up to 89%). The nucleophilic character of the "organo-Ni" intermediates is further exploited to implement a one-pot tricomponent procedure involving the final allylation of aldehydes (yields up to 93%). Mechanistic insights and efficiency on a gram scale process were also documented.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article