Salicylaldehyde-Cobalt(II)-Catalyzed C-H Alkoxylation of Indoles with Secondary Alcohols

被引:5
|
作者
Huang, Mao-Gui [1 ]
Tan, Yu-Yan [1 ]
Ai, Meng-Ting [1 ]
Chen, Xiao-Hong [1 ]
Xu, Hai-Bing [1 ]
Liu, Yue-Jin [1 ]
机构
[1] Hubei Univ, Coll Chem & Chem Engn, Collaborat Innovat Ctr Adv Organ Chem Mat Coconstr, Minist Educ,Key Lab Synth & Applicat Organ Funct M, Wuhan 430062, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 07期
关键词
ASYMMETRIC-SYNTHESIS;
D O I
10.1021/acs.joc.3c02582
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A straight and efficient protocol for the synthesis of hindered indole-ethers via C-H alkoxylation of indoles was developed by a cobalt-catalyzed cross-dehydrogenative coupling reaction with secondary alcohols. The selection of the salicylaldehyde-Co(II) catalyst enables the reaction to proceed under conditions without acid or base addition in the presence of limited alcohols. The protocol has broad substrate scope for both indole and secondary alcohols and exhibits good functional tolerance. The synthetic applications are proven by gram-scale reaction and further diversification of the product. Preliminary mechanistic investigations indicate that the activation of C-H bonds is not the rate-determining step of the reaction.
引用
收藏
页码:4438 / 4443
页数:6
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