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Chiral thiophosphorylated thioureas: Synthesis, structure, and cyclization reaction

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dc.contributor.author Metlushka K.
dc.contributor.author Tufatullin A.
dc.contributor.author Shaimardanova L.
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 2018-09-18T20:13:55Z
dc.date.available 2018-09-18T20:13:55Z
dc.date.issued 2014
dc.identifier.issn 1042-7163
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/137783
dc.description.abstract © 2014 Wiley Periodicals, Inc. A number of chiral racemic and enanthiopure thiophosphorylated thioureas were synthesized by the reaction of 2-aminobutan-1-ol and 1-(a-aminobenzyl)-2-naphthol with O,O-diethyl thiophosphoryl isothiocyanate. It was found that such thioureas undergo the cyclization reaction under basic conditions with hydrogen sulfide elimination and the formation of thiophosphorylated oxasines. XRay single crystal diffraction revealed that the structure of thiourea is close to the prereaction state of the cyclization reaction.
dc.relation.ispartofseries Heteroatom Chemistry
dc.title Chiral thiophosphorylated thioureas: Synthesis, structure, and cyclization reaction
dc.type Article
dc.relation.ispartofseries-issue 6
dc.relation.ispartofseries-volume 25
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 636
dc.source.id SCOPUS10427163-2014-25-6-SID84915771561


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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.

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