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Ni-Catalyzed 1,1- and 1,3-Aminoboration of Unactivated Alkenes.
Lyu, Mao-Yun; Morais, Gabriel N; Chen, Shuming; Brown, M Kevin.
Afiliación
  • Lyu MY; Department of Chemistry, Indiana University, 800 E. Kirkwood Ave, Bloomington, Indiana 47405, United States.
  • Morais GN; Department of Chemistry and Biochemistry, Oberlin College, 119 Woodland St, Oberlin, Ohio 44074, United States.
  • Chen S; Department of Chemistry and Biochemistry, Oberlin College, 119 Woodland St, Oberlin, Ohio 44074, United States.
  • Brown MK; Department of Chemistry, Indiana University, 800 E. Kirkwood Ave, Bloomington, Indiana 47405, United States.
J Am Chem Soc ; 145(50): 27254-27261, 2023 Dec 20.
Article en En | MEDLINE | ID: mdl-38078874
ABSTRACT
Alkene borylfunctionalization reactions have emerged as useful methods for chemical synthesis. While much progress has been made on 1,2-borylamination reactions, the related 1,1- and 1,3-borylaminations have not been reported. Herein, a Ni-catalyzed 1,1-borylamination of 1,1-disubstituted and monosubstituted alkenes and a 1,3-borylamination of cyclic alkenes are presented. Key to development of these reactions was the identification of an alkyllithium activator in combination with Mg salts. The utility of the products and the mechanistic details are discussed.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
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