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Generation of α-Boryl Radicals and Their Conjugate Addition to Enones: Transition-Metal-Free Alkylation of gem-Diborylalkanes.
Wu, Chaoqiang; Bao, Zhicheng; Dou, Bowen; Wang, Jianbo.
Afiliación
  • Wu C; Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of, Ministry of Education, College of Chemistry, Peking University, Beijing, 100871, P. R. China.
  • Bao Z; Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of, Ministry of Education, College of Chemistry, Peking University, Beijing, 100871, P. R. China.
  • Dou B; Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of, Ministry of Education, College of Chemistry, Peking University, Beijing, 100871, P. R. China.
  • Wang J; Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of, Ministry of Education, College of Chemistry, Peking University, Beijing, 100871, P. R. China.
Chemistry ; 27(7): 2294-2298, 2021 Feb 01.
Article en En | MEDLINE | ID: mdl-33064327
ABSTRACT
A transition-metal-free method for the alkylation of gem-diborylalkanes with α,ß-unsaturated ketones has been developed. It is demonstrated that the α-boryl radicals can be generated efficiently from gem-diborylalkanes with the aid of catechol and oxidants. The α-boryl radicals formed through such process can be engaged in conjugate addition reaction with α,ß-unsaturated ketones. This transformation is a straightforward method for the synthesis of γ-borylketones.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article