Application of N-Acylbenzotriazoles in the Synthesis of 5-Substituted 2-Ethoxy-1,3,4-oxadiazoles as Building Blocks toward 3,5-Disubstituted 1,3,4-Oxadiazol-2(3H)-ones

Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/56999

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DC Field	Value	Language
dc.contributor.author	Sirawit Wet-Osot	en_US
dc.contributor.author	Wong Phakhodee	en_US
dc.contributor.author	Mookda Pattarawarapan	en_US
dc.date.accessioned	2018-09-05T03:33:31Z	-
dc.date.available	2018-09-05T03:33:31Z	-
dc.date.issued	2017-01-01	en_US
dc.identifier.issn	15206904	en_US
dc.identifier.issn	00223263	en_US
dc.identifier.other	2-s2.0-85029484222	en_US
dc.identifier.other	10.1021/acs.joc.7b01863	en_US
dc.identifier.uri	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85029484222&origin=inward	en_US
dc.identifier.uri	http://cmuir.cmu.ac.th/jspui/handle/6653943832/56999	-
dc.description.abstract	© 2017 American Chemical Society. 5-Substituted-2-ethoxy-1,3,4-oxadiazoles were conveniently prepared through a one-pot sequential N-acylation/dehydrative cyclization between ethyl carbazate and N-acylbenzotriazoles in the presence of Ph3P-I2as a dehydrating agent. Subsequent treatment with a stoichiometric amount of alkyl halides (X = Cl, Br, I) enables a rapid access to a variety of 3,5-disubstituted 1,3,4-oxadiazol-2(3H)-ones in good to excellent yields.	en_US
dc.subject	Chemistry	en_US
dc.title	Application of N-Acylbenzotriazoles in the Synthesis of 5-Substituted 2-Ethoxy-1,3,4-oxadiazoles as Building Blocks toward 3,5-Disubstituted 1,3,4-Oxadiazol-2(3H)-ones	en_US
dc.type	Journal	en_US
article.title.sourcetitle	Journal of Organic Chemistry	en_US
article.volume	82	en_US
article.stream.affiliations	Chiang Mai University	en_US
Appears in Collections:	CMUL: Journal Articles

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