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Chemoselective synthesis of novel aminoindolizines using aminopyridines, acetylenic diesters and α-halo ketones

Chemoselective synthesis of novel aminoindolizines using aminopyridines, acetylenic diesters and α-halo ketones
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摘要 A chemoselective synthesis of novel indolizine derivatives were reported via three-component reactions of aminopyridines, acetylenic diesters and a-halo ketones. In these reactions, the zwitterion generated from aminopyridines and acetylenic diesters reacted with a-halo ketones to produce indolizine skeleton in good to high yields under mild reaction conditions. A chemoselective synthesis of novel indolizine derivatives were reported via three-component reactions of aminopyridines, acetylenic diesters and a-halo ketones. In these reactions, the zwitterion generated from aminopyridines and acetylenic diesters reacted with a-halo ketones to produce indolizine skeleton in good to high yields under mild reaction conditions.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2016年第3期361-364,共4页 中国化学快报(英文版)
基金 supported by the Research Council of the University of Mazandaran,Iran
关键词 Aminopyridines a-Halo ketones Acetylenic diesters Indolizine Chemoselective synthesis Aminopyridines a-Halo ketones Acetylenic diesters Indolizine Chemoselective synthesis
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