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Metal-free highly chemo-selective bisphosphorylation and deoxyphosphorylation of carboxylic acids.
Gan, Liguang; Xu, Tianhao; Tan, Qihang; Cen, Mengjie; Wang, Lingling; Zhao, Jingwei; Liu, Kuang; Liu, Long; Chen, Wen-Hao; Han, Li-Biao; Nycz, Jacek E; Chen, Tieqiao.
Afiliación
  • Gan L; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Xu T; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Tan Q; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Cen M; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Wang L; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Zhao J; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Liu K; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Liu L; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
  • Chen WH; Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education, College of Chemistry and Chemical Engineering, Hainan Normal University Haikou 571158 China.
  • Han LB; Zhejiang Yangfan New Materials Co. Ltd Shangyu 312369 Zhejiang China hlb@shoufuchem.com.
  • Nycz JE; Institute of Chemistry, Faculty of Science and Technology, University of Silesia in Katowice ul. Szkolna 9 PL-40007 Katowice Poland jacek.nycz@us.edu.pl.
  • Chen T; Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan Provincial Key Lab of Fine Chem, Hainan Provincial Fine Chemical Engineering Research Center, Hainan University Haikou 570228 China chentieqiao@hnu.edu.cn.
Chem Sci ; 14(20): 5519-5526, 2023 May 24.
Article en En | MEDLINE | ID: mdl-37234892
Carboxylic acids are readily available in both the natural and synthetic world. Their direct utilization for preparing organophosphorus compounds would greatly benefit the development of organophosphorus chemistry. In this manuscript, we describe a novel and practical phosphorylating reaction under transition metal-free reaction conditions that can selectively convert carboxylic acids into the P-C-O-P motif-containing compounds through bisphosphorylation, and the benzyl phosphorus compounds through deoxyphosphorylation. This strategy provides a new route for carboxylic acid conversion as the alkyl source, enabling highly efficient and practical synthesis of the corresponding value-added organophosphorus compounds with high chemo-selectivity and wide substrate scope, including the late modification of complex APIs (active pharmaceutical ingredients). Moreover, this reaction also indicates a new strategy for converting carboxylic acids into alkenes by coupling this work and the subsequent WHE reaction with ketones and aldehydes. We anticipate that this new mode of transforming carboxylic acids will find wide application in chemical synthesis.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido