Thioesters as Bifunctional Reagents for 2-Naphthylamine Sulfuracylation

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成果类型：

期刊论文

作者：

Xiao, Fuhong*;Yuan, Shanshan;Wang, Dahan;Liu, Saiwen*;Huang, Huawen;...

通讯作者：

Xiao, Fuhong;Liu, Saiwen

作者机构：

[Yuan, Shanshan; Wang, Dahan; Deng, Guo-Jun; Xiao, Fuhong; Huang, Huawen] Xiangtan Univ, Key Lab Green Organ Synth & Applicat Hunan Prov, Key Lab Environm Friendly Chem & Applicat, Minist Educ,Coll Chem, Xiangtan 411105, Peoples R China.

[Liu, Saiwen] Hunan City Univ, Coll Mat & Chem Engn, Yiyang 413000, Hunan, Peoples R China.

通讯机构：

[Xiao, Fuhong] X

[Liu, Saiwen] H

Xiangtan Univ, Key Lab Green Organ Synth & Applicat Hunan Prov, Key Lab Environm Friendly Chem & Applicat, Minist Educ,Coll Chem, Xiangtan 411105, Peoples R China.

Hunan City Univ, Coll Mat & Chem Engn, Yiyang 413000, Hunan, Peoples R China.

语种：

英文

关键词：

Thioesters;bifunctional;sulfuracylation;diaryl sulfides

期刊：

ADVANCED SYNTHESIS & CATALYSIS

ISSN：

1615-4150

年：

2019

卷：

361

期：

页码：

3331-3336

DOI：

10.1002/adsc.201900301

基金类别：

National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21502160, 21871226, 21572194]; Collaborative Innovation Center of New Chemical Technologies for Environmental Benignity and Efficient Resource Utilization

机构署名：

本校为通讯机构

院系归属：

材料与化学工程学院

摘要：

An efficient and convenient strategy for the preparation of diaryl sulfides via a Fe-promoted direct sulfuracylation of 2-naphthylamine using thioesters as bifunctional reagents is described. This synthetic strategy features high chemoselectivity, good substrate scope and functional group tolerance. (Figure presented.). © 2019 Wi...

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Thioesters as Bifunctional Reagents for 2-Naphthylamine Sulfuracylation

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