Reaction of acyl isocyanates with disubstituted amides and an investigation of hindered internal rotation in amidine molecules

dc.contributor.author	Arbuzov B.
dc.contributor.author	Aganov A.
dc.contributor.author	Zobova N.
dc.contributor.author	Sofronova O.
dc.date.accessioned	2018-09-14T20:32:50Z
dc.date.available	2018-09-14T20:32:50Z
dc.date.issued	1977
dc.identifier.issn	0568-5230
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/132562
dc.description.abstract	1. Trifluoroacetyl isocyanate reacts with dimethylformamide to form a six-membered cycloadduct. Trichloroacetyl isocyanate reacts similarly with dimethylacetamide. 2. Trifluoroacetyl isocyanate reacts with dimethylacetamide to form a substituted 1, 3, 5-dioxazin-4-one, and with dimethylbenzamide to form 1-trifluoroacetyl-2-phenyl-3, 3-dimethylamidine. 3. Using PMR spectroscopy, hindered internal rotation about the {Mathematical expression} bond in amidine molecules has been studied and its kinetic parameters determined. © 1977 Plenum Publishing Corporation.
dc.relation.ispartofseries	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
dc.title	Reaction of acyl isocyanates with disubstituted amides and an investigation of hindered internal rotation in amidine molecules
dc.type	Article
dc.relation.ispartofseries-issue	2
dc.relation.ispartofseries-volume	26
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	348
dc.source.id	SCOPUS05685230-1977-26-2-SID34250291466

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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.