Acetic Acid-Promoted Rhodium(III)-Catalyzed Hydroarylation of Terminal Alkynes

被引:13
|
作者
Duan, Chang-Lin [1 ,2 ]
Liu, Xing-Yu [2 ,4 ]
Tan, Yun-Xuan [2 ]
Ding, Rui [3 ]
Yang, Shiping [1 ]
Tian, Ping [2 ,3 ]
Lin, Guo-Qiang [2 ,3 ]
机构
[1] Shanghai Normal Univ, Dept Chem, 100 Guilin Rd, Shanghai 200234, Peoples R China
[2] Univ Chinese Acad Sci, Chinese Acad Sci, CAS Key Lab Synthet Chem Nat Subst, Ctr Excellence Mol Synth,Shanghai Inst Organ Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Innovat Res Inst Tradit Chinese Med, 1200 Cailun Rd, Shanghai 201203, Peoples R China
[4] ShanghaiTech Univ, Sch Phys Sci & Technol, 100 Haike Rd, Shanghai 201210, Peoples R China
关键词
acetic acid; rhodium catalysis; hydroarylation; alkynes; C-H BONDS; CATALYZED HYDROARYLATION; EFFICIENT ACCESS; ALKENYLATION; ACTIVATION; ARENES; FUNCTIONALIZATION; HETEROCYCLES; MILD;
D O I
10.1055/s-0037-1611780
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Rhodium(III)-catalyzed hydroarylation of terminal alkynes has not previously been achieved because of the inevitable oligomerization and other side reactions. Here, we report a novel Cp* Rh(III)-catalyzed hydroarylation of terminal alkynes in acetic acid as solvent to facilitate the C-H bond activation and subsequent transformations. This reaction proceeds under mild conditions, providing an effective approach to the synthesis of alkenylated heterocycles in high to excellent yields (31-99%) with a broad substrate scope (37 examples) and good functional-group compatibility. In this transformation, the loading of the alkyne can be reduced to 1.2 equivalents, which indicates the significant role of HOAc in lowering the reaction temperature and suppressing the oligomerization of the terminal alkyne. Preliminary mechanistic studies are also presented.
引用
收藏
页码:932 / 938
页数:7
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