Gold(I)-Catalyzed Selective Hydroarylation of Indoles with Haloalkynes

Cunbo Wei; Jiawen Wu; Lizhu Zhang; Zhonghua Xia

doi:10.1021/acs.orglett.2c01921

Gold(I)-Catalyzed Selective Hydroarylation of Indoles with Haloalkynes

Cunbo Wei, Jiawen Wu, Lizhu Zhang, Zhonghua Xia^*

^*此作品的通讯作者

材料学院

Beijing Institute of Technology

科研成果: 期刊稿件 › 文章 › 同行评审

9 引用（Scopus）

摘要

A highly regio- and stereoselective synthesis of a Z-alkenyl indole via the gold-catalyzed addition of an indole to a haloalkyne was developed. In the presence of gold catalyst SIPrAuCl and cocatalyst NaBARF, a broad range of indoles react with haloalkynes to afford Z-alkenyl indoles with high selectivity at room temperature. Computational studies suggest that the hydroarylation reaction takes place via a concerted C2 addition pathway of the indole to the activated haloalkyne. 2022 American Chemical Society.

源语言	英语
页（从-至）	4689-4693
页数	5
期刊	Organic Letters
卷	24
期	25
DOI	https://doi.org/10.1021/acs.orglett.2c01921
出版状态	已出版 - 1 7月 2022

访问文件

10.1021/acs.orglett.2c01921

其它文件与链接

链接到 Scopus 的出版物

引用此

@article{db15ebe36ecc4953a930bd2dbf415573,

title = "Gold(I)-Catalyzed Selective Hydroarylation of Indoles with Haloalkynes",

abstract = "A highly regio- and stereoselective synthesis of a Z-alkenyl indole via the gold-catalyzed addition of an indole to a haloalkyne was developed. In the presence of gold catalyst SIPrAuCl and cocatalyst NaBARF, a broad range of indoles react with haloalkynes to afford Z-alkenyl indoles with high selectivity at room temperature. Computational studies suggest that the hydroarylation reaction takes place via a concerted C2 addition pathway of the indole to the activated haloalkyne. 2022 American Chemical Society.",

author = "Cunbo Wei and Jiawen Wu and Lizhu Zhang and Zhonghua Xia",

year = "2022",

month = jul,

day = "1",

doi = "10.1021/acs.orglett.2c01921",

language = "English",

volume = "24",

pages = "4689--4693",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "25",

}

TY - JOUR

T1 - Gold(I)-Catalyzed Selective Hydroarylation of Indoles with Haloalkynes

AU - Wei, Cunbo

AU - Wu, Jiawen

AU - Zhang, Lizhu

AU - Xia, Zhonghua

PY - 2022/7/1

Y1 - 2022/7/1

N2 - A highly regio- and stereoselective synthesis of a Z-alkenyl indole via the gold-catalyzed addition of an indole to a haloalkyne was developed. In the presence of gold catalyst SIPrAuCl and cocatalyst NaBARF, a broad range of indoles react with haloalkynes to afford Z-alkenyl indoles with high selectivity at room temperature. Computational studies suggest that the hydroarylation reaction takes place via a concerted C2 addition pathway of the indole to the activated haloalkyne. 2022 American Chemical Society.

AB - A highly regio- and stereoselective synthesis of a Z-alkenyl indole via the gold-catalyzed addition of an indole to a haloalkyne was developed. In the presence of gold catalyst SIPrAuCl and cocatalyst NaBARF, a broad range of indoles react with haloalkynes to afford Z-alkenyl indoles with high selectivity at room temperature. Computational studies suggest that the hydroarylation reaction takes place via a concerted C2 addition pathway of the indole to the activated haloalkyne. 2022 American Chemical Society.

UR - http://www.scopus.com/inward/record.url?scp=85133960093&partnerID=8YFLogxK

U2 - 10.1021/acs.orglett.2c01921

DO - 10.1021/acs.orglett.2c01921

M3 - Article

C2 - 35714368

AN - SCOPUS:85133960093

SN - 1523-7060

VL - 24

SP - 4689

EP - 4693

JO - Organic Letters

JF - Organic Letters

IS - 25

ER -

Gold(I)-Catalyzed Selective Hydroarylation of Indoles with Haloalkynes

摘要

访问文件

其它文件与链接

指纹

引用此