首页> 外文期刊>The Journal of Organic Chemistry >One-Pot Cascade Synthesis of Quinazolin-4(3H)-ones via Nickel-Catalyzed Dehydrogenative Coupling of o-Aminobenzamides with Alcohols
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One-Pot Cascade Synthesis of Quinazolin-4(3H)-ones via Nickel-Catalyzed Dehydrogenative Coupling of o-Aminobenzamides with Alcohols

机译:喹唑啉-4(3H) - 氨基唑胺-4(3H)酮的单级级联合成邻氨基苯甲酰胺与醇的脱氢偶联

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摘要

In this paper, we report a general, efficient, and environmentally benign method for the one-pot cascade synthesis of quinazolin-4(3H)-ones via acceptorless dehydrogenative coupling of o-aminobenzamide with alcohols catalyzed by a simple Ni(II) catalyst, [Ni(MeTAA)], featuring a tetraaza macrocyclic ligand (tetramethyltetraaza[14]annulene (MeTAA)). A wide variety of substituted quinazolin-4(3H)-ones were synthesized in high yields starting from readily available benzyl alcohols and o-aminobenzamides. Several controlled reactions along with deuterium labeling studies were carried out to establish the acceptorless dehydrogenative nature of the reactions.
机译:在本文中,我们通过O-氨基酰胺的无氨基酰胺与催化醇催化的醇类脱氢偶联的喹唑啉-4(3H)-4(3H) - 酮的一般,高效和环境良性方法报告了一般,有效和环境良性的喹唑啉-4(3H)-4(3H) - α ,[Ni(MetaA)],具有四氮杂宏环配体(四甲基四氮杂物[14]亚硫(Metaa))。 从易于含苄醇和O-氨基苯甲酰胺开始的高产率合成各种取代的喹唑啉-4(3H)酮。 进行了几种受控反应以及氘标记研究,以确定反应的无可受脱氢性质。

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