Synthesis, polarity, and structure of 2-chloro-N-[2-(methylsulfanyl)phenyl]- and 2-(diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamides

dc.contributor.author	Ishmaeva E.
dc.contributor.author	Alimova A.
dc.contributor.author	Vereshchagina Y.
dc.contributor.author	Chachkov D.
dc.contributor.author	Artyushin O.
dc.contributor.author	Sharova E.
dc.date.accessioned	2018-09-18T20:19:12Z
dc.date.available	2018-09-18T20:19:12Z
dc.date.issued	2015
dc.identifier.issn	1070-4280
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/138673
dc.description.abstract	© 2015 Pleiades Publishing, Ltd. Conformations of 2-chloro-N-[2-(methylsulfanyl)phenyl]- and 2-(diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamides have been studied by the dipole moment method and quantum chemical calculations. 2-(Diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamide has been found to exist as an equilibrium mixture of two conformers with synclinal and anticlinal orientations of the {C-{s{p^3}}} - {C-{s{p^2}}} and P=S bonds. 2-Chloro-N-[2-(methylsulfanyl)phenyl]acetamide is represented by one preferred conformer.
dc.relation.ispartofseries	Russian Journal of Organic Chemistry
dc.title	Synthesis, polarity, and structure of 2-chloro-N-[2-(methylsulfanyl)phenyl]- and 2-(diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamides
dc.type	Article
dc.relation.ispartofseries-issue	7
dc.relation.ispartofseries-volume	51
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	943
dc.source.id	SCOPUS10704280-2015-51-7-SID84939420987

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