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首页> 外文期刊>Journal of the Iranian Chemical Society >Chemoselective Synthesis of 2-Aryloxazines and 2-Aryltetrahydropyrimidines Using Nano-SiO_2 as a Reusable Solid Acid Catalyst under Thermal Conditions and Microwave Irradiation
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Chemoselective Synthesis of 2-Aryloxazines and 2-Aryltetrahydropyrimidines Using Nano-SiO_2 as a Reusable Solid Acid Catalyst under Thermal Conditions and Microwave Irradiation

机译:纳米SiO_2作为可重用固体酸催化剂在热条件和微波辐射下化学选择性合成2-芳基恶嗪和2-芳基四氢嘧啶

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摘要

Nano-SiO_2 solid acid efficiently and selectively catalyzed the cyclocondensation reaction of arylnitriles with 3-amino-1- proopanol or 1,3-diaminopropane to afford their respective 2-substituted oxazines and tetrahydropyrimidines in high yields under thermal conditions and microwave irradiation. This methodology works effectively for the selective synthesis of mono-1,3- oxazines and mono-tetrahydropyrimidnes from dinitriles. The catalyst could be recycled and reused several times without a noticeable decrease in its activity.
机译:纳米SiO_2固体酸可有效地,选择性地催化芳基腈与3-氨基-1-丙醇或1,3-二氨基丙烷的环缩合反应,从而在热条件和微波辐射下高产率地提供各自的2-取代的恶嗪和四氢嘧啶。该方法有效地用于从二腈选择性合成单1,3-恶嗪和单四氢嘧啶。催化剂可以循环使用几次,而活性没有明显下降。

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