Synthesis of Indolizines via Tf2O-Mediated Cascade Reaction of Pyridyl-enaminones with Thiophenols/Thioalcohols

被引:20
作者
Zhang, Changyuan [1 ]
Wang, Wei [1 ]
Zhu, Xuncheng [1 ]
Chen, Lulu [1 ]
Luo, Hejiang [2 ]
Guo, Mengping [1 ]
Liu, Dan [1 ]
Liu, Fan [1 ]
Zhang, Huisheng [1 ]
Li, Qi [1 ]
Lin, Jianping [1 ]
机构
[1] Yichun Univ, Key Lab Jiangxi Univ Appl Chem & Chem Biol, Coll Chem & Bioengn, Yichun 336000, Peoples R China
[2] Kunming Univ Sci & Technol, Fac Life Sci & Technol, Kunming 650500, Peoples R China
关键词
TRIFLIC ANHYDRIDE; ELECTROPHILIC ACTIVATION; AMIDES; TRANSFORMATIONS; TRIFLUOROMETHYLATION; DERIVATIVES; CYCLIZATION; ANNULATION; SECONDARY; KETONES;
D O I
10.1021/acs.orglett.3c00177
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A cost-effective, highly regioselective and metal-free version for the synthesis of indolizine derivatives by means of Tf2O-mediated cascade reaction of pyridyl-enaminones and thiophenols/thioalcohols under mild reaction conditions has been reported. Diverse electron-rich indolizine derivatives could be obtained in up to 94% yield via the selective 1,4-addition of vinyl iminium triflate tandem cyclization/aromatization, which allowed the simultaneous construction of C-N and C-S/and one example of C-Se bonds.
引用
收藏
页码:1192 / 1197
页数:6
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