{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,15]],"date-time":"2026-05-15T07:10:12Z","timestamp":1778829012180,"version":"3.51.4"},"reference-count":45,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T00:00:00Z","timestamp":1764979200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T00:00:00Z","timestamp":1764979200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["ChemistryOpen"],"published-print":{"date-parts":[[2026,4]]},"abstract":"<jats:p>\n                    In this study, the condensation reaction between vinamidinium salts and Z\u20102\u2010hydrazineylidene\u20103\u2010methyl\u20102,3\u2010dihydrobenzo[d]thiazole is described for the synthesis of 1,3\u2010bis((3\u2010methylbenzo[d]thiazol\u20102(3H)\u2010ylidene)hydrazineylidene)propan\u20102\u2010ol (BBTA) or 1\u2010((1Z,3E)\u20101\u2010(dimethylamino)\u20103\u2010(((Z)\u20103\u2010methylbenzo[d]thiazol\u20102(3H)\u2010ylidene)hydrazineylidene)prop\u20101\u2010en\u20102\u2010yl)pyridin\u20101\u2010ium (DMBT). A noteworthy aspect of the synthesis of these derivatives is that the structure of the vinamidinium salt acts as the determining factor for the type of product formed. Specifically, phenyl\u2010substituted vinamidinium salts predominantly lead to the formation of symmetric BBTA derivatives, whereas pyridinium\u2010based vinamidinium salts favor the production of asymmetric DMBT compounds. The reaction was carried out in the presence of triethylamine as the base and acetonitrile as the solvent under catalyst\u2010free conditions. The structure of the new products was confirmed based on their spectral data, including\n                    <jats:sup>1<\/jats:sup>\n                    H NMR,\n                    <jats:sup>13<\/jats:sup>\n                    C NMR, IR, mass spectrometry, high\u2010resolution mass spectrometry and X\u2010ray analysis.\n                  <\/jats:p>","DOI":"10.1002\/open.202500540","type":"journal-article","created":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T13:19:41Z","timestamp":1765027181000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Efficient One\u2010Pot Synthesis of Benzothiazole Compounds From Vinamidinium Salts"],"prefix":"10.1002","volume":"15","author":[{"given":"Zeinab","family":"khosravi","sequence":"first","affiliation":[{"name":"Department of Chemistry Faculty of Nano and Bio Science and Technology Persian Gulf University  Bushehr Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0074-6027","authenticated-orcid":false,"given":"Abdolmohammad","family":"Mehranpour","sequence":"additional","affiliation":[{"name":"Department of Chemistry Faculty of Nano and Bio Science and Technology Persian Gulf University  Bushehr Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammad Reza","family":"Mohammadizadeh","sequence":"additional","affiliation":[{"name":"Department of Chemistry Faculty of Nano and Bio Science and Technology Persian Gulf University  Bushehr Iran"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Genta","family":"Kojya","sequence":"additional","affiliation":[{"name":"Center for Research Advancement and Collaboration University of the Ryukyus  Nishihara Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Satoru","family":"Arimitsuc","sequence":"additional","affiliation":[{"name":"Graduate School of Engineering and Science University of the Ryukyus  Nishihara Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2025,12,6]]},"reference":[{"key":"e_1_2_12_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.tetlet.2004.12.113"},{"key":"e_1_2_12_3_1","doi-asserted-by":"publisher","DOI":"10.2174\/1570179418666210706152515"},{"key":"e_1_2_12_4_1","doi-asserted-by":"publisher","DOI":"10.1039\/D0RA10548A"},{"key":"e_1_2_12_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/jhet.3958"},{"key":"e_1_2_12_6_1","doi-asserted-by":"publisher","DOI":"10.1038\/s41598-024-64179-1"},{"key":"e_1_2_12_7_1","doi-asserted-by":"publisher","DOI":"10.1021\/acs.orglett.1c01725"},{"key":"e_1_2_12_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.tetlet.2019.151002"},{"key":"e_1_2_12_9_1","doi-asserted-by":"publisher","DOI":"10.1039\/D1RA04214A"},{"key":"e_1_2_12_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.tetlet.2014.08.014"},{"key":"e_1_2_12_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.tetlet.2012.11.046"},{"key":"e_1_2_12_12_1","doi-asserted-by":"publisher","DOI":"10.1080\/00397911.2012.681826"},{"key":"e_1_2_12_13_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.tetlet.2014.05.038"},{"key":"e_1_2_12_14_1","doi-asserted-by":"publisher","DOI":"10.1039\/D3RA04309F"},{"key":"e_1_2_12_15_1","first-page":"1707","article-title":"Structural Analysis, In Vitro Anti\u2010Tubercular Activities, And In Silico ADMET Evaluation of Ethyl 7\u2010methoxy\u20103\u2010(4\u2010substituted benzoyl) indolizine\u20101\u2010Carboxylates","volume":"27","author":"Dorai S. 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