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3, 4-二氢嘧啶-2-酮衍生物合成研究进展
引用本文:路军,杨秉勤,白银娟,马怀让.3, 4-二氢嘧啶-2-酮衍生物合成研究进展[J].有机化学,2001,21(9):640-647.
作者姓名:路军  杨秉勤  白银娟  马怀让
作者单位:西北大学化学系,西安,710069
基金项目:陕西省自然科学基金资助课题(No.2000H03)。
摘    要:综述了近十年来3,4-二氢嘧啶-2-酮衍生物合成的研究进展,包括催化合成、固相合成、微波促进合成及天然产物合成中的一些最新研究进展。

关 键 词:固相合成  天然产物  微波辐射  催化反应  嘧啶酮P  合成法
修稿时间:2000年12月6日

Recent advance in the synthesis of 3, 4-dihydropyrimidinones
LU Jun,YANG Bing Qin,BAI Yin Juan,MA Huai Rang.Recent advance in the synthesis of 3, 4-dihydropyrimidinones[J].Chinese Journal of Organic Chemistry,2001,21(9):640-647.
Authors:LU Jun  YANG Bing Qin  BAI Yin Juan  MA Huai Rang
Institution:Northwest Univ, Dept Chem.Xian(710069)
Abstract:The Biginelli reaction, which was first reported more than a century ago, involves the synthesis of 3,4 dihydropyrimidin 2(1 H ) ones of type 4 by a very simple one pot condensation reaction of ethyl acetoacetate, benzaldehyde and urea in ethanol. In the past decade, dihydropyrimidine derivatives have exhibited important pharmacological properties, e.g. as the integral backbones of several calcium channel blockers, antihypertensive agents, alpha 1a antagonists, and neuropeptide Y (NPY) antagonists. In this article, we review development in the Biginelli reaction in the areas such as catalytic synthesis, solid phase synthesis, microwave irradiation, mechanism and natural products synthesis.
Keywords:Biginelli reaction  3  4  dihydropyrimidinones  synthesis  
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