Reaction of 2-acetyl-5-methyl-1, 2, 3-diazaphosphole with diazoacetic ester

dc.contributor.author	Arbuzov B.
dc.contributor.author	Lisin A.
dc.contributor.author	Dianova E.
dc.date.accessioned	2018-09-14T20:41:41Z
dc.date.available	2018-09-14T20:41:41Z
dc.date.issued	1983
dc.identifier.issn	0568-5230
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/132621
dc.description.abstract	Independent of the nature of the solvent, the reaction of 2-acetyl-5-methyl-1,2,3-diazaphosphole with diazoacetic ester proceeds without the evolution of nitrogen to give Δ2-phosphapyrazoline derivatives. The latter in CH2Cl2, CH3CN, or alcohols are isomerized to compounds with two NH groups. © 1984 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-5-methyl-1, 2, 3-diazaphosphole with diazoacetic ester
dc.type	Article
dc.relation.ispartofseries-issue	10
dc.relation.ispartofseries-volume	32
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	2158
dc.source.id	SCOPUS05685230-1983-32-10-SID34250143139

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