首页|Palladium-Catalyzed anti-Markovnikov Halosulfonamidation of Unactivated Alkene

Palladium-Catalyzed anti-Markovnikov Halosulfonamidation of Unactivated Alkene

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Palladium-catalyzed regioselective amination of unactivated alkene remains a challenge and is of great interest.Herein,a three-component coupling of unactivated alkene,sulfonamide,and N-halo compounds accessing vicinal haloamine has been con-ceived.This aminohalogenation represents a modular and regioselective strategy.The electrophilic halogenating agent enables regi-oselective anti-Markovnikov aminopalladation and facilitates subsequent halogenation events.And this protocol is characterized by gram-scale syntheses and late-stage functionalizations.Of note,the recovered byproduct phthalimide allows for reusing by conver-sion to the starting material.

Unactivated alkeneanti-Markovnikov aminopalladationVicinal haloaminePalladium catalysisHalosulfonamidationSelectivityN-Halo compounds

Bowen Wang、Jianxiao Li、Wanqing Wu、Huanfeng Jiang

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State Key Laboratory of Pulp and Paper Engineering,Key Laboratory of Functional Molecular Engineering of Guangdong Province,School of Chemistry and Chemical Engineering,South China University of Technology,Guangzhou,Guangdong 510641,China

国家自然科学基金国家自然科学基金Key-Area Research and Development Program of Guangdong Province

22231002218710952020B010188001

2024

中国化学(英文版)
中国化学会 上海有机化学研究所

中国化学(英文版)

CSTPCD
影响因子:0.848
ISSN:1001-604X
年,卷(期):2024.42(5)
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