Reaction of 2-acetyl-3-methoxy-5-methyldiazaphospholine with p-toluenesulfonyl azide

dc.contributor.author	Arbuzov B.
dc.contributor.author	Dianova E.
dc.contributor.author	Zabotina E.
dc.date.accessioned	2018-09-20T20:44:40Z
dc.date.available	2018-09-20T20:44:40Z
dc.date.issued	1981
dc.identifier.issn	0568-5230
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/146212
dc.description.abstract	Tosyl azide reacts with 2-acetyl-3-methoxy-5-methyldiazaphospholine to give an iminodiazaphospholine that is stable as a solid, while in solutions, depending on the nature of the solvent and the temperature, it changes to the tautomer with an NH bond and the dimer. The equilibrium interconversion of these three forms was shown on the basis of the IR and31P NMR spectra. © 1982 Plenum Publishing Corporation.
dc.relation.ispartofseries	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
dc.title	Reaction of 2-acetyl-3-methoxy-5-methyldiazaphospholine with p-toluenesulfonyl azide
dc.type	Article
dc.relation.ispartofseries-issue	11
dc.relation.ispartofseries-volume	30
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	2192
dc.source.id	SCOPUS05685230-1981-30-11-SID34250232948

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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.