Thiophene-2,5-dicarboxylic acid bis-aryl(alkyl) amides
| dc.contributor.author | Koparir, M | |
| dc.contributor.author | Cansiz, A | |
| dc.contributor.author | Çetin, A | |
| dc.date.accessioned | 2026-08-12T17:13:12Z | |
| dc.date.issued | 2005 | |
| dc.department | Fırat Üniversitesi | |
| dc.description.abstract | A base-catalyzed condensation of diacetamido sulfides [(RNHCOCH2)(2)S)] with glyoxal affording thiophene-2,5-dicarboxylic acid bis-aryl(alkyl)amides has been accomplished under mild conditions. Excellent results were readily obtained when R was a substituted 3-nitrophenyl, 4-nitrophenyl, 4-chlorophenyl group, but the yield was poor when R was cyclohexyl. Unknown compounds were characterized by elemental analyses, IR, H-1, and C-13 NMR techniques. (c) 2005 Wiley Periodicals, Inc. | |
| dc.identifier.doi | 10.1002/hc.20153 | |
| dc.identifier.endpage | 506 | |
| dc.identifier.issn | 1042-7163 | |
| dc.identifier.issue | 6 | |
| dc.identifier.orcid | 0000-0002-3692-6740 | |
| dc.identifier.orcid | 0000-0003-1031-783X | |
| dc.identifier.scopus | 2-s2.0-27744434846 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | 503 | |
| dc.identifier.uri | https://doi.org/10.1002/hc.20153 | |
| dc.identifier.uri | https://hdl.handle.net/11508/51332 | |
| dc.identifier.volume | 16 | |
| dc.identifier.wos | WOS:000231987700008 | |
| dc.identifier.wosquality | Q3 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | John Wiley & Sons Inc | |
| dc.relation.ispartof | Heteroatom Chemistry | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WoS_20260511 | |
| dc.subject | Hinsberg-Reaction | |
| dc.subject | Facile Synthesis | |
| dc.subject | Diketo Sulfides | |
| dc.subject | 2,5-Diacylthiophenes | |
| dc.title | Thiophene-2,5-dicarboxylic acid bis-aryl(alkyl) amides | |
| dc.type | Article |







