Arylhydrazine salt‐selenium: A novel and efficient reagent system for arylselenenylation of unprotected uracil and its derivatives

Author:

Wu Yi1,Peng Qi‐Yun1,He Yan‐Ling2,Zheng Xiao‐He2,Chen Yan‐Qin1,Wang Hai‐Bo3,Wang Bing4,Xie Jun1,Tang Lei5,Wang Cong1

Affiliation:

1. School of Pharmacy, Guizhou Provincial Engineering Technology Research Center for Chemical Drug R&D Guizhou Medical University Guiyang China

2. Research and Development Center Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou China

3. Research and Development Center Zhejiang Hongyuan Pharmaceutical Co., Ltd. Linhai PR China

4. School of Biology and Engineering Guizhou Medical University Guiyang PR China

5. State Key Laboratory of Functions and Applications of Medicinal Plants Guizhou Medical University Guiyang China

Abstract

AbstractA convenient and efficient reagent system of arylhydrazine salt‐selenium was developed to directly selenizing uracil preparation of 5‐selenium uracil. In the presence of this reagent, a variety of uracil/pyrimidine converts to their corresponding 5‐arylselanyluracils/5‐selenopyrimidine with good yield and high regioselectivity. Elemental selenium of commercially accessible, stable, affordable, and easy to use was used as the selenization reagent. This reaction is attractive and practical since there are no catalysts or ligands needed, and a wide range of functional groups can be tolerated.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guizhou Province

Publisher

Wiley

Subject

Organic Chemistry

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