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首页> 外文期刊>Advanced synthesis & catalysis >DBU-Catalyzed [3+3] and [3+2] Annulation Reactions of Azomethine Ylides with -Diazocarbonyls as N-Terminal Electrophiles: Modular, Atom-Economical Access to 1,2,4-Triazine and 1,2,4-Triazole Derivatives
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DBU-Catalyzed [3+3] and [3+2] Annulation Reactions of Azomethine Ylides with -Diazocarbonyls as N-Terminal Electrophiles: Modular, Atom-Economical Access to 1,2,4-Triazine and 1,2,4-Triazole Derivatives

机译:DBU催化[3 + 3]和[3 + 2]与二氮杂羰基的氮杂甲酸钠作为N-末端电泳剂:模块化,原子经济进入1,2,4-三嗪和1,2,4-三唑 衍生品

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摘要

The DBU-catalyzed [3+3] and [3+2] cyclization reactions of azomethine ylides with -diazocarbonyls as N-terminal electrophiles have been developed. These reactions involve a sequential intermolecular nucleophilic addition/intramolecular cyclization/oxidation procedure. By the assembly of readily available starting materials, these transformations offer novel, highly efficient one-pot syntheses of various functionalized 1,2,4-triazine and 1,2,4-triazole derivatives in an atom-economical manner under ambient and metal-free conditions in a high regio- and diastereoselective manner.
机译:已经开发了DBU催化的[3 + 3]和[3 + 2]用-diozoCaronylys作为N-末端电子手机的偶氮甲基氧化物的环化反应。 这些反应涉及连续分子间亲核加成/分子内环化/氧化方法。 通过组装易于获得的原料,这些转化在环境和金属下以原子 - 经济的方式提供新的,高效的一罐合成的各种官能化的1,2,4-三嗪和1,2,4-三唑衍生物 - 自由条件以高序目和非对映选择性的方式。

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