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B(C6F5)3-catalyzed O-H insertion reactions of diazoalkanes with phosphinic acids.
Zhang, Yangyang; Zhang, Xinzhi; Zhao, Jincheng; Jiang, Jun.
Afiliação
  • Zhang Y; College of Chemistry and Chemical Engineering, Guangxi University, Nanning, 530004, P. R. China. jiangjun@gxu.edu.cn.
  • Zhang X; College of Chemistry and Chemical Engineering, Guangxi University, Nanning, 530004, P. R. China. jiangjun@gxu.edu.cn.
  • Zhao J; College of Chemistry and Chemical Engineering, Guangxi University, Nanning, 530004, P. R. China. jiangjun@gxu.edu.cn.
  • Jiang J; College of Chemistry and Chemical Engineering, Guangxi University, Nanning, 530004, P. R. China. jiangjun@gxu.edu.cn and Guangxi Key Laboratory of Electrochemical Energy Materials, Nanning, Guangxi 530004, P. R. China.
Org Biomol Chem ; 19(26): 5772-5776, 2021 Jul 07.
Article em En | MEDLINE | ID: mdl-34137768
ABSTRACT
A highly efficient base-, metal-, and oxidant-free catalytic O-H insertion reaction of diazoalkanes and phosphinic acids in the presence of B(C6F5)3 has been developed. This powerful methodology provides a green approach towards the synthesis of a broad spectrum of α-phosphoryloxy carbonyl compounds with good to excellent yields (up to 99% yield). The protocol features the advantages of operational simplicity, high atom economy, practicality, easy scalability and environmental friendliness.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article