Bismuth-catalyzed methylation and alkylation of quinone derivatives with tert-butyl peroxybenzoate as an oxidant

被引:12
|
作者
Yang, Jian [1 ,2 ]
Dong, Yu [1 ,2 ]
He, Shuai [3 ]
Shi, Zhi-Chuan [3 ]
Wang, Yu [4 ]
Wang, Ji-Yu [1 ]
机构
[1] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Sichuan, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Southwest Minzu Univ, Chengdu 610041, Sichuan, Peoples R China
[4] Guizhou Educ Univ, Guiyang 550018, Guizhou, Peoples R China
关键词
Quinone derivatives; Methylation; Alkylation; Bismuth (III) trifluoromethanesulfonate ten-Butyl peroxybenzoate; C(SP(3))-H BOND FUNCTIONALIZATION; METAL-FREE; OXIDATIVE CYCLIZATION; ARYLATION; ACCESS; ALLYLATION; THYMOQUINONE; CINNAMAMIDES; AMINATION; SULFONES;
D O I
10.1016/j.tet.2019.130729
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A bismuth-catalyzed methylation of quinones in the presence of tert-butyl peroxybenzoate (TBPB) was developed via a radical reaction mechanism. Particularly, TBPB was used not only as an efficient oxidant, but also as a green methyl source in such transformation. Moreover, this method could also be efficiently extended to the alkylation of quinones. This reaction tolerated a series of functional groups and prepared a series of derivatives of vitamin K-3 and benzoquinone. Notably, antimalarial parvaquone was synthesized by the reaction. (C) 2019 Elsevier Ltd. All rights reserved.
引用
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页数:7
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