Investigation on the Ring-Opening Reactions of 3-(1H-1,2,4-Triazol-1-yl)1,5-benzothiazepines with Arylonitrile Oxides |
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Authors: | Sheng-Qin Chen Fei Ding Fang-Ming Liu |
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Institution: | 1. College of Materials and Chemical Engineering , Hangzhou Normal University , Hangzhou , P.R. China;2. Technology Center of Juhua Group , Quzhou , P.R. China |
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Abstract: | Abstract Novel ring opening compounds, (Z)-2-((Z)-((E)-1,3-diaryl-2-(1H-1,2,4-triazol-1-yl)allylidene)amino)aryl N-hydroxybenzimidothioates 4a–r, were obtained from the reaction of 2,4-diaryl-3-(1H-1,2,4-triazol-1-yl)-2,5-dihydro-1,5-benzothiazepines 3a–f and arylonitrile oxides. The structure of these products has been elucidated by spectroscopic analysis and, in one case, X-ray crystallographic analysis. According to the result, it was presumed that this reaction did not proceeded through 1,3-dipolar cycloaddition reaction. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. GRAPHICAL ABSTRACT ![id=](/na101/home/literatum/publisher/tandf/journals/content/gpss20/2011/gpss20.v186.i03/10426507.2010.509290/20170126/images/medium/gpss_a_509290_o_uf0001.gif) |
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Keywords: | Arylcarbohydroximinoyl chloride benzothiazepine ring-opening 1 2 4-triazole |
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