Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles

被引:3
|
作者
Peshkov, Anatoly A. [1 ,2 ]
Gapanenok, Diana [1 ]
Puzyk, Aleksandra [1 ]
Amire, Niyaz [2 ]
Novikov, Alexander S. [1 ,3 ]
Martynova, Sofia D. [1 ]
Kalinin, Stanislav [1 ]
Dar'in, Dmitry [1 ]
Peshkov, Vsevolod A. [2 ]
Krasavin, Mikhail [1 ,4 ]
机构
[1] St Petersburg State Univ, Inst Chem, St Petersburg 199034, Russia
[2] Nazarbayev Univ, Sch Sci & Humanities, Dept Chem, Nur Sultan 010000, Kazakhstan
[3] Peoples Friendship Univ Russia, RUDN Univ, Res Inst Chem, Moscow 117198, Russia
[4] Immanuel Kant Balt Fed Univ, Kaliningrad 236016, Russia
来源
JOURNAL OF ORGANIC CHEMISTRY | 2023年 / 88卷 / 15期
关键词
CATALYST-FREE APPROACH; AZA-ENE REACTION; KETENE AMINALS; REGIOSELECTIVE SYNTHESIS; MULTICOMPONENT REACTIONS; CASCADE REACTION; C-C; DERIVATIVES; EFFICIENT; FACILE;
D O I
10.1021/acs.joc.3c00497
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A chemoselective strategy toward a variety of fused heterocyclicscaffolds relying on a three-component condensation of heterocyclicketene aminals (HKAs) or corresponding thioaminals with aryl glyoxalsand cyclic 1,3-dicarbonyl compounds has been developed and explored.Depending on the applied combination of substrates, the strategy canbe tuned to provide straightforward access to imidazo[1,2-a]quinoline, pyrrolo[1,2-a]imidazole, andpyrrolo[2,1-b]thiazole frameworks.
引用
收藏
页码:10508 / 10524
页数:17
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