Synthesis of aminobismethylenephosphonic acids on a platform of p-tert-Butylthiacalix[4]arene in 1,3-alternate configuration

dc.contributor.author	Shibaeva K.
dc.contributor.author	Nazarova A.
dc.contributor.author	Kuznetsova D.
dc.contributor.author	Stoikov I.
dc.date.accessioned	2018-09-19T21:00:26Z
dc.date.available	2018-09-19T21:00:26Z
dc.date.issued	2016
dc.identifier.issn	1070-3632
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/143502
dc.description.abstract	© 2016, Pleiades Publishing, Ltd.Aminobismethylenephosphonic acids on a platform of p-tert-butylthiacalix[4]arene were obtained by reacting macrocyclic amines with phosphorous acid and formaldehyde under acid catalysis. Free phenol hydroxy groups on the lower rim of p-tert-butylthiacalix[4]arene were found to inhibit the interaction with the amino moieties of the macrocycle. In the case of amino derivatives of thiacalix[4]arene containing no hydroxy groups the reaction led to the formation of target compounds in good yields.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.subject	aminobismethylenephosphonic acid
dc.subject	bisphosphonates
dc.subject	calixarenes
dc.subject	phosphorylation
dc.subject	thiacalix[4]-arene derivatives
dc.title	Synthesis of aminobismethylenephosphonic acids on a platform of p-tert-Butylthiacalix[4]arene in 1,3-alternate configuration
dc.type	Article
dc.relation.ispartofseries-issue	3
dc.relation.ispartofseries-volume	86
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	579
dc.source.id	SCOPUS10703632-2016-86-3-SID84969631069

Files in this item

Size: 43.79Kb

Format: PDF

Публикации сотрудников КФУ Scopus [24551]
Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.