Copper(i)-catalyzed multicomponent interrupted click reaction: modular synthesis of triazole sulfides from elemental sulfur

被引:11
|
作者
Sun, Pengfei [1 ]
Wang, Weiguo [3 ]
Lai, Jilong [1 ]
Yan, Huang [1 ]
Tung, Chen-Ho [1 ]
Xu, Zhenghu [1 ,2 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Educ Minist, Jinan 250100, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[3] Qufu Normal Univ, Sch Chem & Chem Engn, Jining, Peoples R China
关键词
OXIDATIVE TRIFLUOROMETHYLTHIOLATION; REGIOSELECTIVE SYNTHESIS; TERMINAL ALKYNES; CYCLOADDITION; 1,2,3-TRIAZOLES; CHEMISTRY; LIGATION; CARBON; AZIDES; ACIDS;
D O I
10.1039/d3qo00224a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Organic synthesis of complex molecules from basic chemicals is one of the most attractive approaches. We report herein the development of a new multicomponent copper(i)-catalyzed interrupted click reaction which allows the rapid modular synthesis of multi-substituted triazole sulfides from elemental sulfur. The generation of an active electrophilic sulfuration reagent by the activation of elemental sulfur is the major feature of this method. The interception of the click intermediate cuprate-triazole with a sulfur electrophile formed in situ allows the modular synthesis of 5-thio and 5-selenotriazoles including various medium-sized cycles and macrocycles in one step with absolute regioselectivity.
引用
收藏
页码:1890 / 1896
页数:7
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