{"title":"摘要/ Abstract摘要:含叠氮基团的芳香前体通过分子间和分子内环加成合成多种苯并三唑。","authors":"Suguru Yoshida, Takamoto Morita, Takamitsu Hosoya","doi":"10.1002/chin.201652267","DOIUrl":null,"url":null,"abstract":"<p>Starting from 3-(azidoalkoxy)aryne precursor, a diverse range of bis-1,2,3-triazoles (IV) are obtained via a sequential azide-alkyne and azide-aryne cycloaddition, while unique ring-fused benzotriazoles (VI) are obtained via an intramolecular azido-aryne cycloaddition.</p>","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652267","citationCount":"0","resultStr":"{\"title\":\"ChemInform Abstract: Synthesis of Diverse Benzotriazoles from Aryne Precursors Bearing an Azido Group via Inter- and Intramolecular Cycloadditions.\",\"authors\":\"Suguru Yoshida, Takamoto Morita, Takamitsu Hosoya\",\"doi\":\"10.1002/chin.201652267\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Starting from 3-(azidoalkoxy)aryne precursor, a diverse range of bis-1,2,3-triazoles (IV) are obtained via a sequential azide-alkyne and azide-aryne cycloaddition, while unique ring-fused benzotriazoles (VI) are obtained via an intramolecular azido-aryne cycloaddition.</p>\",\"PeriodicalId\":9834,\"journal\":{\"name\":\"ChemInform\",\"volume\":\"47 52\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-12-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/chin.201652267\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemInform\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/chin.201652267\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemInform","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/chin.201652267","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
ChemInform Abstract: Synthesis of Diverse Benzotriazoles from Aryne Precursors Bearing an Azido Group via Inter- and Intramolecular Cycloadditions.
Starting from 3-(azidoalkoxy)aryne precursor, a diverse range of bis-1,2,3-triazoles (IV) are obtained via a sequential azide-alkyne and azide-aryne cycloaddition, while unique ring-fused benzotriazoles (VI) are obtained via an intramolecular azido-aryne cycloaddition.
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