Yıldırım, MuhammetÇelikel, DeryaEvis, NaciyeKnight, David W.Kariuki, Benson M.2021-06-232021-06-2320140040-4020https://doi.org/10.1016/j.tet.2014.06.070https://hdl.handle.net/20.500.12491/7804Base-catalyzed one-pot cyclocondensation reactions of acryloyl and cinnamoyl chlorides with beta-nitroenamine derivatives have been performed under mild conditions and target 7-substituted thiazolo-[3,2-alpha] or imidazolo-[1,2-alpha]pyridin-5-one derivatives were prepared successfully in moderate to good yields. The cyclization reactions may proceed via Michael addition followed by iminoketene-amide tautomerization in view of the products formed. (C) 2014 Elsevier Ltd. All rights reserved.eninfo:eu-repo/semantics/closedAccessHeterocyclic NitroenamineOne-pot ReactionMulticomponentMichael AdditionCinnamoyl ChloridesArticle10.1016/j.tet.2014.06.0707035567456812-s2.0-84949157226Q2WOS:000340336000038Q2