首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of Azolo[1,3,5]triazines via Rhodium(III)-Catalyzed Annulation of N-Azolo Imines and Dioxazolones
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Synthesis of Azolo[1,3,5]triazines via Rhodium(III)-Catalyzed Annulation of N-Azolo Imines and Dioxazolones

机译:通过Rhodium(III)的亚沙罗[1,3,5]三嗪的合成 - 催化N-唑醇亚胺和Dioxazolones

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摘要

A wide range of azolo[1,3,5]triazines were obtained by Rh(III)-catalyzed annulation of N-azolo imines and dioxazolones. The reaction proceeds by the first catalytic C-H amidation of an imidoyl C-H bond followed by cyclodehydration. Good yields were obtained for N-azolo imines derived from aminoazoles and aromatic and heteroaromatic aldehydes. A range of dioxazolone amidating reagents were employed to introduce aryl, heteroaryl, and alkyl substituents. The reaction was also performed with a benchtop setup at 1 mmol scale using microwave heating.
机译:通过RH(III)获得了各种Azolo [1,3,5]三嗪 - 催化N-唑醇亚胺和Dioxazolones的催化。 反应通过第一催化C-H酰胺化的IMIDOYL C-H键,然后环氢化水合进行。 获得源自氨基氮杂胺和芳族醛和杂芳醛的N-Azolo亚胺的良好产量。 使用一系列二氧氮杂胺酰胺化试剂引入芳基,杂芳基和烷基取代基。 还使用微波加热以1mmol刻度的台式设定进行反应。

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