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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Unprecedented formation of benzo[d][1,2,3,6]oxatriazocine derivatives via diazo-oxygen bond formation and synthesis of enantiomerically pure 1-alkyl benzotriazole derivatives
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Unprecedented formation of benzo[d][1,2,3,6]oxatriazocine derivatives via diazo-oxygen bond formation and synthesis of enantiomerically pure 1-alkyl benzotriazole derivatives

机译:通过重氮-氧键的形成和对映体纯的1-烷基苯并三唑衍生物的合成,前所未有地形成苯并[d] [1,2,3,6]草三唑胺衍生物

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摘要

A series of amino acid-derived enantiomerically pure substituted benzo[d][1,2,3,6]oxatriazocine derivatives and 1-alkyl substituted benzotriazoles has been prepared by the diazotization of amino acid-derived benzo-fused alicycles. The first unprecedented diazo-oxygen bond formation in acidic medium led to an entirely new kind of substituted benzo[d][1,2,3,6]oxatriazocine heterocycles.
机译:通过氨基酸衍生的苯并稠合的脂环族的重氮化,制备了一系列氨基酸衍生的对映体纯的苯并[d] [1,2,3,6]恶三唑胺衍生物和1-烷基取代的苯并三唑。在酸性介质中第一个前所未有的重氮-氧键形成导致了一种全新的取代苯并[d] [1,2,3,6]恶三唑嗪杂环。

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