| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1257497 | Chinese Chemical Letters | 2012 | 4 Pages |
Abstract
A novel route for the synthesis of thiazolo[3,2-a]pyrimidin-7-ones and pyrido[1,2-a]pyrimidin-2-ones from acetylated 2-aminothiazoles and 2-aminopyridines under Vilsmeier conditions has been developed. The plausible mechanism has also been proposed.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
![A novel and convenient synthesis of thiazolo[3,2-a]pyrimidin-7-ones and pyrido[1,2-a]pyrimidin-2-ones using Vilsmeier reagent](/preview/png/1257497.png "First Page Preview: A novel and convenient synthesis of thiazolo[3,2-a]pyrimidin-7-ones and pyrido[1,2-a]pyrimidin-2-ones using Vilsmeier reagent")
Authors
Yi Yi Weng, Lei Ming Ying, Qi Xu Chen, Wei Ke Su,