Rhodium(III)-Catalyzed Intramolecular Annulation and Aromatization for the Synthesis of Pyrrolo[1,2-a]quinolines

被引:9
作者
Hu, Yongchun [1 ,2 ]
Jia, Yuanyuan [3 ]
Tuo, Zekun [1 ,2 ]
Zhou, Wang [1 ,2 ,3 ]
机构
[1] Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China
[2] Hunan Normal Univ, Key Lab Assembly & Applicat Organ Funct Mol Hunan, Changsha 410081, Peoples R China
[3] Xiangtan Univ, Coll Chem Engn, Xiangtan 411105, Peoples R China
基金
中国国家自然科学基金;
关键词
PALLADIUM-CATALYZED ANNULATION; C BOND FORMATION; INTERNAL ALKYNES; H ACTIVATION; ACCESS; FUNCTIONALIZATION; PYRROLOQUINOLINES; HYDROCARBONS; CYCLIZATION; QUINOLINES;
D O I
10.1021/acs.orglett.3c00321
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A rhodium(III)-catalyzed protocol for the synthesis of pyrrolo[1,2-a]quinolines through intramolecular annulation of o-alkynyl amino aromatic ketones and subsequent aromatization is reported. This transformation builds the pyrrole and quinoline moieties of the pyrrolo[1,2-a]quinoline in one pot and achieves a flexible introduction of different substituent groups at 4- and 5-positions on products that were difficult to prepare by other means. The reaction proceeds smoothly on a gram scale, and the products are amenable to downstream synthetic manipulations.
引用
收藏
页码:1845 / 1849
页数:5
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