Base-promoted new C-C bond formation: an expedient route for the preparation of thiazolo- and imidazolo-pyridinones via Michael addition
dc.authorid | 0000-0002-8658-3897 | en_US |
dc.contributor.author | Yıldırım, Muhammet | |
dc.contributor.author | Çelikel, Derya | |
dc.contributor.author | Evis, Naciye | |
dc.contributor.author | Knight, David W. | |
dc.contributor.author | Kariuki, Benson M. | |
dc.date.accessioned | 2021-06-23T19:35:30Z | |
dc.date.available | 2021-06-23T19:35:30Z | |
dc.date.issued | 2014 | |
dc.department | BAİBÜ, Fen Edebiyat Fakültesi, Kimya Bölümü | en_US |
dc.description.abstract | Base-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. | en_US |
dc.identifier.doi | 10.1016/j.tet.2014.06.070 | |
dc.identifier.endpage | 5681 | en_US |
dc.identifier.issn | 0040-4020 | |
dc.identifier.issue | 35 | en_US |
dc.identifier.scopus | 2-s2.0-84949157226 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 5674 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.tet.2014.06.070 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12491/7804 | |
dc.identifier.volume | 70 | en_US |
dc.identifier.wos | WOS:000340336000038 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.institutionauthor | Yıldırım, Muhammet | |
dc.institutionauthor | Çelikel, Derya | |
dc.institutionauthor | Evis, Naciye | |
dc.language.iso | en | en_US |
dc.publisher | Pergamon-Elsevier Science Ltd | en_US |
dc.relation.ispartof | Tetrahedron | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Heterocyclic Nitroenamine | en_US |
dc.subject | One-pot Reaction | en_US |
dc.subject | Multicomponent | en_US |
dc.subject | Michael Addition | en_US |
dc.subject | Cinnamoyl Chlorides | en_US |
dc.title | Base-promoted new C-C bond formation: an expedient route for the preparation of thiazolo- and imidazolo-pyridinones via Michael addition | en_US |
dc.type | Article | en_US |
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