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Synthesis of spiro thiazolo[3,2-a]pyrimidine compounds by one-pot sequential 1,3-dipolar cycloadditions

✍ Scribed by Xiaofang Li; Aiting Zheng; Bin Liu; Guobin Li; Xianyong Yu; Pinggui Yi


Publisher
Journal of Heterocyclic Chemistry
Year
2011
Tongue
English
Weight
95 KB
Volume
48
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

A new class of spiro thiazolo[3,2‐a]pyrimidine compounds were synthesized by the one‐pot sequential 1,3‐dipolar cycloaddition of azomethine ylide (generated from isatin and sarcosine)–nitrile oxide to 2‐arylmethylidene‐6,7‐dihydro‐5__H__‐thiazolo[3,2‐a]pyrimidin‐3‐ones in moderate yields. The structures of all the products were characterized thoroughly by NMR, MS, IR, elemental analysis, and NMR together with X‐ray crystallographic analysis. J. Heterocyclic Chem., (2011).


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