Effect of the alkylidene spacer and the p-tert-butylthiacalix[4]arene macrocyclic platform on the reactivity of the hydroxyl groups in the acylation reaction

dc.contributor.author	Padnya P.
dc.contributor.author	Bayarashov E.
dc.contributor.author	Potrekeeva O.
dc.contributor.author	Stoikov I.
dc.date.accessioned	2018-04-05T07:09:38Z
dc.date.available	2018-04-05T07:09:38Z
dc.date.issued	2017
dc.identifier.issn	1070-3632
dc.identifier.uri	http://dspace.kpfu.ru/xmlui/handle/net/129875
dc.description.abstract	© 2017, Pleiades Publishing, Ltd. A series of cone and 1,3-alternate p-tert-butylthiacalix[4]arenes tetrasubstituted at the lower rim simultaneously by the amide, ester, and carboxyl functions were synthesized. The reactivity of the synthesized compounds depends on the length of the alkylidene spacer. The N-(hydroxyethyl)amide derivatives do not react with succinic anhydride, whereas the N-(3-hydroxypropyl)amide derivatives react to form acylation products.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.subject	macrocycles
dc.subject	succinic anhydride
dc.subject	thiacalix[4]arene
dc.title	Effect of the alkylidene spacer and the p-tert-butylthiacalix[4]arene macrocyclic platform on the reactivity of the hydroxyl groups in the acylation reaction
dc.type	Letter
dc.relation.ispartofseries-issue	9
dc.relation.ispartofseries-volume	87
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	2111
dc.source.id	SCOPUS10703632-2017-87-9-SID85031898848

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Публикации сотрудников КФУ Scopus [24551]
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