A new synthetic route to chiral 3-aryl-5-ethyl-1,4,2-oxazaphosphorines

dc.contributor.author	Metlushka K.
dc.contributor.author	Sadkova D.
dc.contributor.author	Nikitina K.
dc.contributor.author	Yamaleeva Z.
dc.contributor.author	Ivshin K.
dc.contributor.author	Kataeva O.
dc.contributor.author	Alfonsov V.
dc.date.accessioned	2019-01-22T20:39:01Z
dc.date.available	2019-01-22T20:39:01Z
dc.date.issued	2018
dc.identifier.issn	0959-9436
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/148130
dc.description.abstract	© 2018 Diastereoselective synthesis of racemic and enantiopure 3-aryl-5-ethyl-1,4,2-oxazaphosphorines, including those bearing phenolic hydroxyl groups in the exocyclic aromatic fragment, was implemented by the reaction of imines derived from (±)-and (R)-(−)-2-aminobutan-1-ol and (hydroxy)benzaldehydes with triethyl phosphite and trifluoroacetic acid, followed by the one-pot dealkylation of the intermediate esters.
dc.relation.ispartofseries	Mendeleev Communications
dc.title	A new synthetic route to chiral 3-aryl-5-ethyl-1,4,2-oxazaphosphorines
dc.type	Article
dc.relation.ispartofseries-issue	6
dc.relation.ispartofseries-volume	28
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	579
dc.source.id	SCOPUS09599436-2018-28-6-SID85057745764

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