Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on 1,3-dipolar cycloaddition

dc.contributor.author	Burilov V.
dc.contributor.author	Epifanova N.
dc.contributor.author	Popova E.
dc.contributor.author	Vasilevsky S.
dc.contributor.author	Solovieva S.
dc.contributor.author	Antipin I.
dc.contributor.author	Konovalov A.
dc.date.accessioned	2018-09-18T20:17:38Z
dc.date.available	2018-09-18T20:17:38Z
dc.date.issued	2013
dc.identifier.issn	1066-5285
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/138392
dc.description.abstract	Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on the 1,3-dipolar cycloaddition of substituted benzyl azides to tetra(propargyloxy)calix[4]arenes in the presence of copper iodide was carried out. The presence of the p-methoxybenzyl substituent in the triazole ring leads to a dramatic (more than tenfold) increase in the fluorescence of the corresponding macrocycle in a region of 290-310 nm. © 2013 Springer Science+Business Media New York.
dc.relation.ispartofseries	Russian Chemical Bulletin
dc.subject	1,2,3-triazoles
dc.subject	1,3-dipolar cycloaddition
dc.subject	benzyl azides
dc.subject	calix[4]arenes
dc.subject	fluorescence
dc.title	Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on 1,3-dipolar cycloaddition
dc.type	Article
dc.relation.ispartofseries-issue	3
dc.relation.ispartofseries-volume	62
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	767
dc.source.id	SCOPUS10665285-2013-62-3-SID84891815156

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