Ligand-controlled Regiodivergent C-H Alkenylation of Pyrazoles and its Application to the Synthesis of Indazoles

被引:42
|
作者
Kim, Hyun Tae [1 ,2 ]
Ha, Hyeri [1 ,2 ]
Kang, Geunhee [1 ,2 ]
Kim, Og Soon [1 ,2 ]
Ryu, Ho [3 ,4 ]
Biswas, Abul Kalam [3 ,4 ]
Lim, Sang Min [5 ,6 ]
Baik, Mu-Hyun [3 ,4 ]
Joo, Jung Min [1 ,2 ]
机构
[1] Pusan Natl Univ, Dept Chem, Busan 46241, South Korea
[2] Pusan Natl Univ, Chem Inst Funct Mat, Busan 46241, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[4] Inst for Basic Sci Korea, Ctr Catalyt Hydrocarbon Functionalizat, Daejeon 34141, South Korea
[5] Korea Inst Sci & Technol, Ctr Neuromed, Brain Sci Inst, Seoul 02792, South Korea
[6] Korea Univ Sci & Technol, Div Biomed Sci & Technol, Daejeon 34113, South Korea
基金
新加坡国家研究基金会;
关键词
alkenylation; C-H activation; indazole; palladium; pyrazole; AMINO-ACID LIGANDS; DIRECT ARYLATION; ACTIVATION; FUNCTIONALIZATION; OXIDATION; MECHANISM; INDOLES; ARENES; AZOLES; ROUTE;
D O I
10.1002/anie.201709162
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Regioselective C4-, C5-, and di-alkenylations of pyrazoles were achieved. An electrophilic Pd catalyst generated by trifluoroacetic acid (TFA) and 4,5-diazafluoren-9-one (DAF) leads to C4-alkenylation, whereas KOAc and mono-protected amino acid (MPAA) ligand Ac-Val-OH give C5-alkenylation. A combination of palladium acetate, silver carbonate, and pivalic acid affords dialkenylation products. Annulation through sequential alkenylation, thermal 6 pi-electrocyclization, and oxidation gives functionalized indazoles. This comprehensive strategy greatly expands the range of readily accessible pyrazole and indazole derivatives, enabling useful regiodivergent C-H functionalization of pyrazoles and other heteroaromatic systems.
引用
收藏
页码:16262 / 16266
页数:5
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