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题名

Organocatalytic Enantioselective Aza-Michael Addition of Arylamines to 7-Methide-7H-Indoles

作者
通讯作者Li,Pengfei; Dong,Mingxin; Li,Wenjun
发表日期
2021
DOI
发表期刊
ISSN
1615-4150
EISSN
1615-4169
卷号363页码:2557-2561
摘要

A chiral phosphorus acid catalyzed enantioselective 1,4-conjugate addition of arylamines to in situ formed 7-methylene-7H-indoles from 7-indolylmethanols has been developed for the first time. Without additives, the catalytic protocol enabled the formation of 1,4-adducts with a nitrogen-containing tertiary carbon stereocenter in 66–96% yield with 70–89% ee under mild conditions. (Figure presented.).

关键词
相关链接[Scopus记录]
收录类别
语种
英语
学校署名
通讯
资助项目
Special Funds of the Taishan Scholar Program of Shandong Province[tsqn201812047] ; Natural Science Foundation of Shandong Province[ZR2017JL011] ; Guangdong Provincial Key Laboratory of Catalysis[2020B121201002]
WOS研究方向
Chemistry
WOS类目
Chemistry, Applied ; Chemistry, Organic
WOS记录号
WOS:000630392500001
出版者
Scopus记录号
2-s2.0-85103016767
来源库
Scopus
引用统计
被引频次[WOS]:12
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/222788
专题理学院_化学系
深圳格拉布斯研究院
作者单位
1.Department of Medicinal Chemistry,School of Pharmacy,Qingdao University,Qingdao,Shandong,266021,China
2.Shenzhen Grubbs Institute and Department of Chemistry,Guangdong Provincial Key Laboratory of Catalysis,Southern University of Science and Technology,Shenzhen,518055,China
3.Department of Immunology,School of Basic Medicine,Qingdao University,Qingdao,266021,China
通讯作者单位化学系;  深圳格拉布斯研究院
推荐引用方式
GB/T 7714
Li,Fushuai,Yang,Zhihong,Yang,Yanyan,et al. Organocatalytic Enantioselective Aza-Michael Addition of Arylamines to 7-Methide-7H-Indoles[J]. ADVANCED SYNTHESIS & CATALYSIS,2021,363:2557-2561.
APA
Li,Fushuai.,Yang,Zhihong.,Yang,Yanyan.,Huang,Qiuhong.,Chen,Xuling.,...&Li,Wenjun.(2021).Organocatalytic Enantioselective Aza-Michael Addition of Arylamines to 7-Methide-7H-Indoles.ADVANCED SYNTHESIS & CATALYSIS,363,2557-2561.
MLA
Li,Fushuai,et al."Organocatalytic Enantioselective Aza-Michael Addition of Arylamines to 7-Methide-7H-Indoles".ADVANCED SYNTHESIS & CATALYSIS 363(2021):2557-2561.
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