Reactions of 5,7-dichloro-4,6-dinitrobenzofuroxane and -furazane with triphenylphosphine

dc.contributor.author	Galkina I.
dc.contributor.author	Tudrii E.
dc.contributor.author	Berdnikov E.
dc.contributor.author	Yusupova L.
dc.contributor.author	Levinson F.
dc.contributor.author	Krivolapov D.
dc.contributor.author	Litvinov I.
dc.contributor.author	Cherkasov R.
dc.contributor.author	Galkin V.
dc.date.accessioned	2018-09-18T20:19:04Z
dc.date.available	2018-09-18T20:19:04Z
dc.date.issued	2012
dc.identifier.issn	1070-4280
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/138649
dc.description.abstract	Reactions of 5,7-dichloro-4,6-dinitrobenzofuroxane and 5,7-dichloro-4,6- dinitrobenzofurazane with triphenylphosphine proceed through a nucleophilic aromatic substitution of chlorine and nitro groups in the six-membered ring of the heterocycles. The structure of the phosphorylation products was established from the IR, 31P NMR, and mass spectra and from XRD and elemental analysis. Schemes of the routes of the phosphorylation are discussed. © 2012 Pleiades Publishing, Ltd.
dc.relation.ispartofseries	Russian Journal of Organic Chemistry
dc.title	Reactions of 5,7-dichloro-4,6-dinitrobenzofuroxane and -furazane with triphenylphosphine
dc.type	Article
dc.relation.ispartofseries-issue	5
dc.relation.ispartofseries-volume	48
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	721
dc.source.id	SCOPUS10704280-2012-48-5-SID84863712620

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