Reaction of pyridoxal and its azomethines with hydrophosphoryl compounds

dc.contributor.author	Kibardina L.
dc.contributor.author	Trifonov A.
dc.contributor.author	Dobrynin A.
dc.contributor.author	Pudovik M.
dc.contributor.author	Pudovik E.
dc.contributor.author	Burilov A.
dc.date.accessioned	2018-09-19T20:48:52Z
dc.date.available	2018-09-19T20:48:52Z
dc.date.issued	2016
dc.identifier.issn	1042-6507
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/143302
dc.description.abstract	© 2016 Taylor & Francis Group, LLC.The products of carbonyl phosphonylation of pyridoxal with alkylphosphinic acid ethyl esters, phosphorous acid dialkyl esters have been obtained for the first time. In some cases, the products of addition are hydrolytically unstable and stabilize by forming internal betaine structures. The reaction of pyridoxal with phosphorous acid in alcohol solutions gives alkoxyfuropyridines possessing the iminium nitrogen atom.
dc.relation.ispartofseries	Phosphorus, Sulfur and Silicon and the Related Elements
dc.subject	Alkylphosphinic acid ethyl esters
dc.subject	dialkylphosphinous acids
dc.subject	phosphorous acid
dc.subject	phosphorus acid dialkyl esters
dc.subject	pyridoxal
dc.title	Reaction of pyridoxal and its azomethines with hydrophosphoryl compounds
dc.type	Article
dc.relation.ispartofseries-issue	11-12
dc.relation.ispartofseries-volume	191
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1599
dc.source.id	SCOPUS10426507-2016-191-1112-SID84992669686

Файлы в этом документе

Размер: 43.75Kb

Формат: 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.