Silver-Promoted Regioselective Oxidative Decarboxylative C-H Alkylation of Phenanthridines with Carboxylic Acids

被引:5
|
作者
Huang, Tianyin [1 ]
Yu, Yang [1 ]
Wang, Hui [1 ]
Lin, Yifan [1 ]
Ma, Yurui [1 ]
Wang, Haoyu [1 ]
Ding, Chang-Hua [1 ]
Xiao, Junjie [1 ]
Xu, Bin [1 ,2 ]
机构
[1] Shanghai Univ, Sch Life Sci, Qianweichang Coll, Dept Chem,Innovat Drug Res Ctr, Shanghai 200444, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
来源
SYNTHESIS-STUTTGART | 2020年 / 52卷 / 02期
基金
中国国家自然科学基金;
关键词
phenanthridine; decarboxylation; silver acetate; C-H alkylation; potassium persulfate; late-stage modification; ISOCYANIDE INSERTION; 6-SUBSTITUTED PHENANTHRIDINES; RADICAL REACTIONS; CYCLIZATION; ACCESS; DERIVATIVES; ISONITRILES; ACTIVATION; ANNULATION; CYANATION;
D O I
10.1055/s-0039-1690220
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel oxidative decarboxylative C-H alkylation of phenanthridines with carboxylic acids was developed for the efficient synthesis of multi-substituted phenanthridine derivatives. The given method features easy availability of starting materials, high regioselectivity, and mild conditions. Furthermore, a one-pot synthesis of multi-substituted phenanthridine derivatives was realized by the reaction of biphenyl isocyanides and carboxylic acid.
引用
收藏
页码:239 / 245
页数:7
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