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Tunable vicinal, geminal diphosphorylation and C-N bond phosphorylation of enaminones toward divergent phosphorylated ketone derivatives.
Cao, Dingsheng; Wang, Chaoli; Wan, Jie-Ping; Wen, Chengping; Liu, Yunyun.
Afiliación
  • Cao D; National Engineering Research Center for Carbohydrate Synthesis, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, China. chemliuyunyun@jxnu.edu.cn.
  • Wang C; National Engineering Research Center for Carbohydrate Synthesis, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, China. chemliuyunyun@jxnu.edu.cn.
  • Wan JP; National Engineering Research Center for Carbohydrate Synthesis, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, China. chemliuyunyun@jxnu.edu.cn.
  • Wen C; Institute of Basic Research in Clinical Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China. wengcp@yeah.net.
  • Liu Y; National Engineering Research Center for Carbohydrate Synthesis, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, China. chemliuyunyun@jxnu.edu.cn.
Chem Commun (Camb) ; 59(42): 6383-6386, 2023 May 23.
Article en En | MEDLINE | ID: mdl-37157911
ABSTRACT
This paper reports the trifunctionalization reactions of tertiary enaminones in the fashion of selective gem- and vicinal diphosphorylation, leading to the tunable synthesis of α,α- and α,ß-diphosphoryl ketones. In addition, the C-N bond phosphorylation with improved substrate tolerance has been achieved.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: China