Iridium-Catalyzed, Weakly Coordination-Assisted Ortho-Alkynylation of (Hetero)aromatic Carboxylic Acids without Cyclization

被引:54
作者
Chen, Changpeng [1 ]
Liu, Pei [1 ]
Tang, Jinghua [1 ]
Deng, Gongda [1 ]
Zeng, Xiaoming [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710054, Peoples R China
[2] Sichuan Univ, Coll Chem, Key Lab Green Chem & Technol, Minist Educ, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H ALKYNYLATION; TRACELESS DIRECTING GROUPS; BENZOIC-ACIDS; C(SP(2))-H BONDS; ORTHO-ARYLATION; PALLADIUM; ARENES; ARYL; ALKYNES; FUNCTIONALIZATIONS;
D O I
10.1021/acs.orglett.7b00581
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
It is reported a weakly coordination-assisted alkynylation of aryl and heteroaryl carboxylic acids with iridium catalysis. The reaction is catalyzed by [{Cp*IrCl2}(2)] complex without cyclization, forming ortho-alkynylated aryl and heteroaryl carboxylic acids, and features high functional group tolerance and broad substrate scope under an air atmosphere. 2-(Hetero)aryl-substituted acetic acids were amenable to the alkynylation by forming an unusual six-membered ring cycloiridiated intermediate.
引用
收藏
页码:2474 / 2477
页数:4
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