Direct aminosulfonylation of electron-rich (hetero)arenes utilizing tert-butyl chlorosulfonylcarbamate and diisopropylethylamine
文献类型:期刊论文
作者 | Zhang, Xiaofei2; Tan, Jiangtao2,3; Zhong, Yuancheng2; Zhuang, Zhen2,3; He, Qian2![]() ![]() |
刊名 | ORGANIC CHEMISTRY FRONTIERS
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出版日期 | 2024-11-19 |
页码 | 8 |
ISSN号 | 2052-4129 |
DOI | 10.1039/d4qo01731e |
通讯作者 | Jiang, Min(jiangm263@163.com) ; Yang, Chunhao(chyang@simm.ac.cn) |
英文摘要 | Sulfonamides, especially primary aryl sulfonamides, are very important scaffolds not only because of their wide applications as pharmacophores in drugs, but also their derivatization into other sulfonamides and different sulfur-containing compounds. Among aryl sulfonamides, most syntheses of electron-rich (hetero)aryl sulfonamides are still severely limited by the classic chlorosulfonation or oxidative chlorination reactions with significant drawbacks. In this work, using the proposed and unique tert-butyl sulfonylcarbamate intermediate generated in situ from easily accessible tert-butyl chlorosulfonylcarbamate and diisopropylethylamine, a catalyst-free, mild and very practical aminosulfonylation protocol for a wide range of electron-rich (hetero)arene substrates with good to excellent yields was reported. |
WOS关键词 | N-SULFONYLAMINES ; SULFONAMIDES ; INHIBITOR ; POLYMERIZATION ; SULFONATION ; ACID ; ARYL |
资助项目 | State Key Laboratory of Drug Research[LG202103-01-06] ; [SKLDR-2023-KF-06] |
WOS研究方向 | Chemistry |
语种 | 英语 |
WOS记录号 | WOS:001363497900001 |
出版者 | ROYAL SOC CHEMISTRY |
源URL | [http://119.78.100.183/handle/2S10ELR8/314668] ![]() |
专题 | 中国科学院上海药物研究所 |
通讯作者 | Jiang, Min; Yang, Chunhao |
作者单位 | 1.Shanghai Jiao Tong Univ, Sch Med, Shanghai Key Lab Prevent & Treatment Bone & Joint, Shanghai Inst Traumatol & Orthopaed,Ruijin Hosp,De, 197 Ruijin 2nd Rd, Shanghai 200025, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Mat Med, Dept Med Chem, State Key Lab Drug Res, 555 Zu Chong Zhi Rd, Shanghai 201203, Peoples R China 3.Univ Chinese Acad Sci, Sch Pharm, 19A Yuquan Rd, Beijing 100049, Peoples R China |
推荐引用方式 GB/T 7714 | Zhang, Xiaofei,Tan, Jiangtao,Zhong, Yuancheng,et al. Direct aminosulfonylation of electron-rich (hetero)arenes utilizing tert-butyl chlorosulfonylcarbamate and diisopropylethylamine[J]. ORGANIC CHEMISTRY FRONTIERS,2024:8. |
APA | Zhang, Xiaofei.,Tan, Jiangtao.,Zhong, Yuancheng.,Zhuang, Zhen.,He, Qian.,...&Yang, Chunhao.(2024).Direct aminosulfonylation of electron-rich (hetero)arenes utilizing tert-butyl chlorosulfonylcarbamate and diisopropylethylamine.ORGANIC CHEMISTRY FRONTIERS,8. |
MLA | Zhang, Xiaofei,et al."Direct aminosulfonylation of electron-rich (hetero)arenes utilizing tert-butyl chlorosulfonylcarbamate and diisopropylethylamine".ORGANIC CHEMISTRY FRONTIERS (2024):8. |
入库方式: OAI收割
来源:上海药物研究所
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