Betti base in the synthesis of chiral bisphosphorylated thioureas

dc.contributor.author	Metlushka K.
dc.contributor.author	Sadkova D.
dc.contributor.author	Nikitina K.
dc.contributor.author	Lodochnikova O.
dc.contributor.author	Kataeva O.
dc.contributor.author	Alfonsov V.
dc.date.accessioned	2018-04-05T07:09:39Z
dc.date.available	2018-04-05T07:09:39Z
dc.date.issued	2017
dc.identifier.issn	1070-3632
dc.identifier.uri	http://dspace.kpfu.ru/xmlui/handle/net/129885
dc.description.abstract	© 2017, Pleiades Publishing, Ltd. Phosphorylation of a naphthol hydroxy group of thiophosphorylated thiourea obtained by reaction of diethyl thiophosphoryl isothiocyanate with 1-(α-aminobenzyl)-2-naphthol (Betti base) afforded a number of chiral bisphosphorylated thioureas. Molecular structure of the obtained compounds was studied by single crystal X-ray diffraction. The capacity of the studied compounds for dimerization due to the intermolecular N–HS hydrogen bonding was revealed.
dc.relation.ispartofseries	Russian Journal of General Chemistry
dc.subject	Betti base
dc.subject	intra- and intermolecular interactions
dc.subject	O-phosphorylation
dc.subject	packing polymorphism
dc.subject	thiophosphorylated thioureas
dc.title	Betti base in the synthesis of chiral bisphosphorylated thioureas
dc.type	Article
dc.relation.ispartofseries-issue	9
dc.relation.ispartofseries-volume	87
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1893
dc.source.id	SCOPUS10703632-2017-87-9-SID85031938187

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Публикации сотрудников КФУ Scopus [24551]
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