An improved protocol on the synthesis of thiazolo[3,2-a]pyrimidine using ultrasonic probe irradiation

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DC Field	Value	Language
dc.contributor.author	Sian Hui Tan
dc.contributor.author	Tse Seng Chuah
dc.contributor.author	Poh Wai Chia
dc.date.accessioned	2017-04-11T05:00:48Z
dc.date.available	2017-04-11T05:00:48Z
dc.date.issued	2016
dc.identifier.citation	Vol.60(4); 245-250 p.	en_US
dc.identifier.issn	10172548
dc.identifier.uri	http://hdl.handle.net/123456789/5727
dc.description.abstract	An improved protocol on the synthesis of thiazolo[3,2-a]pyrimidine-6-carboxylate derivatives are reported. Previously, the thiazolo[3,2-a]pyrimidine-6-carboxylate derivatives were prepared in a two-step procedure. Under the improved procedure, the thiazolo[3,2-a]pyrimidine-6-carboxylate derivatives was readily prepared in a one-step reaction. This procedure was found to be more efficient than the previous protocol and also compared to the ultrasound bath and conventional heating methods in terms of yield and reaction time.	en_US
dc.language.iso	en	en_US
dc.publisher	Journal of the Korean Chemical Society	en_US
dc.subject	One-pot three component synthesis	en_US
dc.subject	Thiazolo[3,2-a]pyrimidine	en_US
dc.subject	Ultrasound	en_US
dc.subject	Solvent- and catalyst-free reaction	en_US
dc.title	An improved protocol on the synthesis of thiazolo[3,2-a]pyrimidine using ultrasonic probe irradiation	en_US
dc.type	Article	en_US
Appears in Collections:	Journal Articles

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