Reaction of carbonyl-stabilized selenonium ylides with derivatives of some group V trivalent elements

dc.contributor.author	Arbuzov B.
dc.contributor.author	Belkin Y.
dc.contributor.author	Polezhaeva N.
dc.contributor.author	Buslaeva G.
dc.date.accessioned	2018-09-20T20:43:18Z
dc.date.available	2018-09-20T20:43:18Z
dc.date.issued	1979
dc.identifier.issn	0568-5230
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/146196
dc.description.abstract	1. The "iodonium method" is an efficient way of synthesizing the selenonium ylides: 2-methylphenylselenuranylidenedimedon and methylphenylselenuranylidenedibenzoylmethane. 2. Similar to S-alkyl-substituted sulfonium ylides, 2-methylphenylselenuranylidenedimedon and methylphenylselenuraaylidenedibenzoylmethane when treated with Et3N or Ph3As in the presence of NaBPh4 are demethylated to give the corresponding ammonium and arsonium tetraphenylborates. © 1979 Plenum Publishing Corporation.
dc.relation.ispartofseries	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
dc.title	Reaction of carbonyl-stabilized selenonium ylides with derivatives of some group V trivalent elements
dc.type	Article
dc.relation.ispartofseries-issue	5
dc.relation.ispartofseries-volume	28
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1072
dc.source.id	SCOPUS05685230-1979-28-5-SID34250272713

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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.