Divergent synthesis of functionalized thioethers via multicomponent reaction of benzynes

被引：21
|
作者：
Jian, Hui [1 ]
Wang, Qiang [1 ]
Wang, Wei-Hua [1 ]
Li, Zhi-Juan [1 ]
Gu, Cheng-Zhi [1 ]
Dai, Bin [1 ]
He, Lin [1 ]
机构：
[1] Shihezi Univ, Sch Chem & Chem Engn, Key Lab Green Proc Chem Engn Xinjiang Bingtuan, Shihezi 832000, Xinjiang Uygur, Peoples R China
来源：
TETRAHEDRON | 2018年 / 74卷 / 23期
基金：
中国国家自然科学基金;
关键词：
Benzyne; Thioether; Multicomponent reaction; CARBON-SULFUR BONDS; CROSS-COUPLING REACTION; DIELS-ALDER REACTION; C-C BOND; FORMING REACTIONS; TANDEM REACTION; ARYNES; CONSTRUCTION; SULFIDES; INSERTION;
D O I：
10.1016/j.tet.2018.04.072
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Diverse functionalized thioethers were efficiently synthesized through the multicomponent reaction of benzynes, cyclic thioethers and different nucleophiles. Both inorganic salts (KF, KC1, KBr, and KSCN) and silylated reagents (TMSCN, TMSN3, TMSCI can be utilized as efficient nucleophiles for the reaction. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码：2876 / 2883
页数：8
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