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This m\u00fcnchnone showed low reactivity as dipole although from the reaction with dimethyl acetylenedicarboxylate the corresponding (3<jats:italic>R<\/jats:italic>)\u20103\u2010phenyl\u201017<jats:italic>H<\/jats:italic>,3<jats:italic>H<\/jats:italic>\u2010pyrrolo[1,2\u2010<jats:italic>c<\/jats:italic>]thiazole\u20105,6,7\u2010tricarboxylate could be isolated. The thermolysis of (2<jats:italic>R<\/jats:italic>,4<jats:italic>R<\/jats:italic>)\u2010<jats:italic>N<\/jats:italic>\u2010ethoxyoxalyl\u20102\u2010phenylthiazolidine\u20104\u2010carboxylic acid in refluxing acetic anhydride led to the synthesis of <jats:italic>N<\/jats:italic>\u2010(1\u2010ethoxycarbonyl\u20102\u2010phenylvinyl)\u20102\u2010phenyl\u20104\u2010thioxo\u20101,3\u2010thiazolidine. The structure of methyl (2<jats:italic>R<\/jats:italic>,4<jats:italic>R<\/jats:italic>)\u2010<jats:italic>N<\/jats:italic>\u2010ethoxyoxalyl\u20102\u2010phenylthiazoliddine\u20104\u2010carboxylate was determined by X\u2010ray crystallography.<\/jats:p>","DOI":"10.1002\/jhet.5570410403","type":"journal-article","created":{"date-parts":[[2009,3,11]],"date-time":"2009-03-11T06:12:33Z","timestamp":1236751953000},"page":"493-497","source":"Crossref","is-referenced-by-count":5,"title":["Generation and reactivity of 3\u2010carbethoxy\u20105\u2010phenyl\u2010<i>5H,7H<\/i>\u2010thiazolo[3,4\u2010<i>c<\/i>]oxazol\u20104\u2010ium\u20101\u2010olate"],"prefix":"10.1002","volume":"41","author":[{"given":"Teresa M. V. D.","family":"Pinho e Melo","sequence":"first","affiliation":[]},{"given":"Clara S. B.","family":"Gomes","sequence":"additional","affiliation":[]},{"given":"Maria I. 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