Nickel-catalyzed regio- And diastereoselective hydroarylative and hydroalkenylative cyclization of 1,6-dienes

Zhengshuai Xu; Yitian Tang; Chaoren Shen; Hongru Zhang; Yuxin Gan; Xiaolei Ji; Xinxin Tian; Kaiwu Dong

doi:10.1039/c9cc09450d

Nickel-catalyzed regio- And diastereoselective hydroarylative and hydroalkenylative cyclization of 1,6-dienes

Zhengshuai Xu
, Yitian Tang
, Chaoren Shen
, Hongru Zhang
, Yuxin Gan
, Xiaolei Ji
, Xinxin Tian
, Kaiwu Dong^*

^*此作品的通讯作者

化学与分子工程学院

East China Normal University
Shanxi University

科研成果: 期刊稿件 › 文章 › 同行评审

6 引用（Scopus）

摘要

An unprecedented nickel-catalyzed hydroarylative and hydroalkenylative cyclization of unsymmetrically substituted 1,6-dienes with organoboronic acid was developed by using MeOH as the hydrogen source and employing commercially available Ni(η2-1,5-cyclooctadiene)2 as the catalyst. A series of biologically interesting cyclic products were afforded in moderate to excellent yields with high regio- and diastereoselectivities.

源语言	英语
页（从-至）	7741-7744
页数	4
期刊	Chemical Communications
卷	56
期	56
DOI	https://doi.org/10.1039/c9cc09450d
出版状态	已出版 - 18 7月 2020

访问文件

10.1039/c9cc09450d

其它文件与链接

链接到 Scopus 的出版物

引用此

@article{b7b39135587d4827bf89f098f33b3c40,

title = "Nickel-catalyzed regio- And diastereoselective hydroarylative and hydroalkenylative cyclization of 1,6-dienes",

abstract = "An unprecedented nickel-catalyzed hydroarylative and hydroalkenylative cyclization of unsymmetrically substituted 1,6-dienes with organoboronic acid was developed by using MeOH as the hydrogen source and employing commercially available Ni(η2-1,5-cyclooctadiene)2 as the catalyst. A series of biologically interesting cyclic products were afforded in moderate to excellent yields with high regio- and diastereoselectivities.",

author = "Zhengshuai Xu and Yitian Tang and Chaoren Shen and Hongru Zhang and Yuxin Gan and Xiaolei Ji and Xinxin Tian and Kaiwu Dong",

note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry.",

year = "2020",

month = jul,

day = "18",

doi = "10.1039/c9cc09450d",

language = "英语",

volume = "56",

pages = "7741--7744",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "56",

}

TY - JOUR

T1 - Nickel-catalyzed regio- And diastereoselective hydroarylative and hydroalkenylative cyclization of 1,6-dienes

AU - Xu, Zhengshuai

AU - Tang, Yitian

AU - Shen, Chaoren

AU - Zhang, Hongru

AU - Gan, Yuxin

AU - Ji, Xiaolei

AU - Tian, Xinxin

AU - Dong, Kaiwu

PY - 2020/7/18

Y1 - 2020/7/18

N2 - An unprecedented nickel-catalyzed hydroarylative and hydroalkenylative cyclization of unsymmetrically substituted 1,6-dienes with organoboronic acid was developed by using MeOH as the hydrogen source and employing commercially available Ni(η2-1,5-cyclooctadiene)2 as the catalyst. A series of biologically interesting cyclic products were afforded in moderate to excellent yields with high regio- and diastereoselectivities.

AB - An unprecedented nickel-catalyzed hydroarylative and hydroalkenylative cyclization of unsymmetrically substituted 1,6-dienes with organoboronic acid was developed by using MeOH as the hydrogen source and employing commercially available Ni(η2-1,5-cyclooctadiene)2 as the catalyst. A series of biologically interesting cyclic products were afforded in moderate to excellent yields with high regio- and diastereoselectivities.

UR - https://www.scopus.com/pages/publications/85088179738

U2 - 10.1039/c9cc09450d

DO - 10.1039/c9cc09450d

M3 - 文章

C2 - 32558829

AN - SCOPUS:85088179738

SN - 1359-7345

VL - 56

SP - 7741

EP - 7744

JO - Chemical Communications

JF - Chemical Communications

IS - 56

ER -

Nickel-catalyzed regio- And diastereoselective hydroarylative and hydroalkenylative cyclization of 1,6-dienes

摘要

访问文件

其它文件与链接

指纹

引用此