Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines

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DC Field	Value	Language
dc.contributor.author	Wong Phakhodee	en_US
dc.contributor.author	Sirilak Wangngae	en_US
dc.contributor.author	Nittaya Wiriya	en_US
dc.contributor.author	Mookda Pattarawarapan	en_US
dc.date.accessioned	2018-09-05T02:53:45Z	-
dc.date.available	2018-09-05T02:53:45Z	-
dc.date.issued	2016-01-01	en_US
dc.identifier.issn	18733581	en_US
dc.identifier.issn	00404039	en_US
dc.identifier.other	2-s2.0-84994028119	en_US
dc.identifier.other	10.1016/j.tetlet.2016.10.069	en_US
dc.identifier.uri	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994028119&origin=inward	en_US
dc.identifier.uri	http://cmuir.cmu.ac.th/jspui/handle/6653943832/55261	-
dc.description.abstract	© 2016 Elsevier Ltd A convenient one-pot protocol for the synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines is reported. In the presence of the Ph3P–I2/Et3N system, a variety of secondary amides were smoothly reacted with primary or secondary amines to afford the corresponding amidines in good to excellent yields under mild conditions.	en_US
dc.subject	Biochemistry, Genetics and Molecular Biology	en_US
dc.subject	Chemistry	en_US
dc.subject	Pharmacology, Toxicology and Pharmaceutics	en_US
dc.title	Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines	en_US
dc.type	Journal	en_US
article.title.sourcetitle	Tetrahedron Letters	en_US
article.volume	57	en_US
article.stream.affiliations	Chiang Mai University	en_US
Appears in Collections:	CMUL: Journal Articles

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