首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >H_3PW_(12)0_(40): An Efficient and Recyclable Heterogeneous Catalyst for the Selective Synthesis of 2-Aryl-5,6-dihydro-4H-1,3-oxazines and 2-Aryl-1,4,5,6-tetrahydropyrimidines
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H_3PW_(12)0_(40): An Efficient and Recyclable Heterogeneous Catalyst for the Selective Synthesis of 2-Aryl-5,6-dihydro-4H-1,3-oxazines and 2-Aryl-1,4,5,6-tetrahydropyrimidines

机译:H_3PW_(12)0_(40):选择性合成2-Aryl-5,6-dihydro-4H-1,3-oxazines和2-Aryl-1,4,5,6-的高效且可回收的多相催化剂四氢嘧啶

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摘要

An environmentally friendly and highly efficient procedure has been developed for the selective synthesis of 2-aryl-5,6-dihydro-4H-1,3-oxazines and 2-aryl-1,4,5,6-tetrahydropyrimidines by cyclocondensation of arylnitriles with 3-amino- 1-propanol and 1,3-diaminopropane in the presence of catalytic amPoWu_(nts of H_3PW 12)O_(40)under thermal conditions and MW irradiation. Under the same reaction conditions, dicyanobenzenes are transformed to their corresponding mono-oxazines and monotetrahydropyrimidines with excellent chemoselectivity. These reactions are simple and clean, giving the products in high yields and high purity. The catalyst can be easily recovered after the reaction and reused efficiently in subsequent runs.
机译:通过芳基腈的环缩合反应,选择性合成2-芳基-5,6-二氢-4H-1,3-恶嗪和2-芳基-1,4,5,6-四氢嘧啶的环保,高效方法已得到开发。在热条件和微波辐射下,在催化的amPoWu_(H_3PW 12的nts)O_(40)存在下,用3-氨基-1-丙醇和1,3-二氨基丙烷。在相同的反应条件下,二氰基苯以优异的化学选择性转化为其相应的单恶嗪和单四氢嘧啶。这些反应简单而干净,使产物具有高产率和高纯度。反应后,催化剂可以很容易地回收,并在随后的运行中有效地再利用。

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