Iodine-Catalyzed Regioselective Sulfenylation of Indoles with Thiols in Water

被引：15

作者：

He, Yongqin ^{[1
]}

Liu, Shengkang ^{[1
]}

Wen, Ping ^{[2
]}

Tian, Wanfa ^{[1
]}

Ren, Xiaoyu ^{[1
]}

Zhou, Qiangxiao ^{[1
]}

Ma, Haojie ^{[1
]}

Huang, Guosheng ^{[1
]}

机构：

[1] Lanzhou Univ, Dept Chem, State Key Lab Appl Organ Chem, Key Lab Nonferrous Met Chem & Resources Utilizat, Lanzhou, Peoples R China

[2] Baoji Univ Arts & Sci, Dept Chem Engn, Baoji 721016, Peoples R China

来源：

CHEMISTRYSELECT | 2016年 / 1卷 / 08期

关键词：

EFFICIENT SULFENYLATION; ARYLTHIOINDOLES; SYSTEM; OXONE; MONO;

D O I：

10.1002/slct.201600257

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A novel protocol of Iodine catalyzed oxidative 3-sulfenylation of indoles with thiols has been developed using cheap and environment friendly Hydrogen peroxide (30% H2O2) as oxidant. In addition, H2O was firstly used as solvent in this type of reaction, in this method, indoles react with multiple thiols smoothly and various 3-sulfanylindoles were obtained in good to excellent yields.. The extensive scope of substrates, the mild reaction conditions, and the high selection of reaction site delivery promising applications in drug discovery and functional materials. Especially, Indole-1-carboxamides were also compatible with this transformation, and the predictable products were obtained in good yields.

引用

页码：1567 / 1570

页数：4

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