版权说明 操作指南
首页 > 成果 > 详情

Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes

认领
导出
Link by DOI
反馈
分享
QQ微信 微博
成果类型:
期刊论文
作者:
Wu, Yan-Dong*;Ma, Jun-Rui;Shu, Wen-Ming;Zheng, Kai-Lu;Wu, An-Xin*吴安心
通讯作者:
Wu, Yan-Dong;Wu, An-Xin(吴安心
作者机构:
[Wu, An-Xin; Wu, Yan-Dong; Ma, Jun-Rui; Zheng, Kai-Lu; Shu, Wen-Ming] Cent China Normal Univ, Minist Educ, Coll Chem, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.
通讯机构:
[Wu, YD; Wu, AX] C
Cent China Normal Univ, Minist Educ, Coll Chem, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.
语种:
英文
关键词:
2,3-Disubstituted indoles;Base-promoted domino reaction;2-Aminobenzaldehyde/2-amino aryl ketones;Tosylhydrazine;Aromatic aldehydes
期刊:
Tetrahedron
ISSN:
0040-4020
年:
2016
卷:
72
期:
32
页码:
4821-4826
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21272085, 21472056]; Excellent Doctorial Dissertation Cultivation Grant from Central China Normal University [2015YBYB053]
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
A base-promoted domino reaction to synthesize the 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes has been developed. This strategy provides a simple and beneficial way for the construction of 2,3-disubstituted indole compounds from readily available s...

反馈

验证码:
看不清楚,换一个
确定
取消

成果认领

标题:
用户 作者 通讯作者
请选择
请选择
确定
取消

提示

该栏目需要登录且有访问权限才可以访问

如果您有访问权限,请直接 登录访问

如果您没有访问权限,请联系管理员申请开通

管理员联系邮箱:yun@hnwdkj.com