Cinchona Alkaloids in the Synthesis of Chiral Salts of Phosphorus Dithioacids on the Basis of 1,2:3,4-Di-O-isopropylidene-α-D-galactopyranose

dc.contributor.author	Nizamov I.
dc.contributor.author	Shumatbaev G.
dc.contributor.author	Salikhov R.
dc.contributor.author	Nikitin Y.
dc.contributor.author	Shulaeva M.
dc.contributor.author	Pozdeev O.
dc.contributor.author	Batyeva E.
dc.contributor.author	Cherkasov R.
dc.date.accessioned	2020-01-15T22:07:02Z
dc.date.available	2020-01-15T22:07:02Z
dc.date.issued	2019
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/156657
dc.description.abstract	© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Optically active dithiophosphoric and dithiophosphonic acids were obtained by the reactions of 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose with tetraphosphorus decasulfide or Lawesson's reagent respectively. The reactions of dithiophosphoric and dithiophosphonic acids with 8 S,9R-quinine, 8R,9 S-quinidine, 8 S,9R-cinchonidine, 8R,9 S-cinchonine, and 8R,9 S-hydroquinidine result in chiral salts of dithiophosphoric and dithiophosphonic acids. Antimicrobial activity of products obtained was tested.
dc.subject	antimicrobial activity
dc.subject	chiral salts
dc.subject	cinchona alkaloids
dc.subject	monosaccharides
dc.subject	phosphorus dithioacids
dc.title	Cinchona Alkaloids in the Synthesis of Chiral Salts of Phosphorus Dithioacids on the Basis of 1,2:3,4-Di-O-isopropylidene-α-D-galactopyranose
dc.type	Article
dc.relation.ispartofseries-issue	5
dc.relation.ispartofseries-volume	4
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1681
dc.source.id	SCOPUS-2019-4-5-SID85061199351

Файлы в этом документе

Размер: 48.41Kb

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.