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在二乙胺水溶液介质中进行的串联羟醛-迈克尔反应:一种更绿色高效地合成双嘧啶衍生物的方法。

Tandem aldol-Michael reactions in aqueous diethylamine medium: a greener and efficient approach to bis-pyrimidine derivatives.

作者信息

Al-Majid Abdullah M, Barakat Assem, Al-Najjar Hany J, Mabkhot Yahia N, Ghabbour Hazem A, Fun Hoong-Kun

机构信息

Department of Chemistry, Faculty of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.

出版信息

Int J Mol Sci. 2013 Dec 5;14(12):23762-73. doi: 10.3390/ijms141223762.

Abstract

A simple protocol, involving the green synthesis for the construction of novel bis-pyrimidine derivatives, 3a-i and 4a-e are accomplished by the aqueous diethylamine media promoted tandem Aldol-Michael reaction between two molecules of barbituric acid derivatives 1a,b with various aldehydes. This efficient synthetic protocol using an economic and environmentally friendly reaction media with versatility and shorter reaction time provides bis-pyrimidine derivatives with high yields (88%-99%).

摘要

一种简单的方法,涉及用于构建新型双嘧啶衍生物3a-i和4a-e的绿色合成,通过在水二乙胺介质中促进巴比妥酸衍生物1a、b的两个分子与各种醛之间的串联羟醛-迈克尔反应来实现。这种使用经济且环境友好的反应介质、具有通用性且反应时间较短的高效合成方法,能以高收率(88%-99%)提供双嘧啶衍生物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd1c/3876076/9983636b11b3/ijms-14-23762f1.jpg

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