版权说明 操作指南
首页 > 成果 > 详情

New efficient synthesis of isoquinoline-1,3(2H,4H)-diones and isoindolin-1-ones via sequential Ugi/cyclization reaction

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:
Yuan, Ding;Duan, Zhuan;Rao, Yong;Ding, Ming -Wu*
通讯作者:
Ding, Ming -Wu
作者机构:
[Duan, Zhuan; Rao, Yong; Ding, Ming -Wu; Yuan, Ding] Cent China Normal Univ, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.
通讯机构:
[Ding, Ming -Wu] C
Cent China Normal Univ, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.
语种:
英文
关键词:
Acid catalyst;Base catalyzed reaction;Isoindolin-1-one;Isoquinoline-1,3(2H,4H)-dione;Ugi reaction
期刊:
Tetrahedron
ISSN:
0040-4020
年:
2016
卷:
72
期:
2
页码:
338-346
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21572075, 21172085]
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 new efficient synthesis of isoquinoline-1,3(2H,4H)-diones or isoindolin-1-ones via sequential Ugi-4CR or Ugi-3CR/cyclization reaction was developed. α-Acylamino amides 5, obtained from Ugi-4CR of methyl 2-formylbenzoate, amines, isocyanates and acids, cyclized to give isoquinoline-1,3(2H,4H)-diones 6 in good yields in the presence of catalytic amount of sodium ethoxide. Ugi-3CR of methyl 2-formylbenzoate, amines and isocyanates in the presence of catalytic amount of H3P...

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