Reaction of 2-tert-butoxy-4,5-benzo-1,3,2-dioxaphospholane with tribromoacetaldehyde

dc.contributor.author	Sinyashina T.
dc.contributor.author	Mironov V.
dc.contributor.author	Ofitserov E.
dc.contributor.author	Konovalova I.
dc.contributor.author	Pudovik A.
dc.date.accessioned	2018-09-14T20:46:15Z
dc.date.available	2018-09-14T20:46:15Z
dc.date.issued	1989
dc.identifier.issn	0568-5230
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/132698
dc.description.abstract	The reaction of 2-tert-butoxy-4,5-benzo-1,3,2-dioxaphospholane with tribromo-acetaldehyde proceeds by initial halophilic attack on the bromine atom, leading to a product with retention of the P-Br bond (pyrocatechol bromophosphate) and an anion exchange product (pyrocatechol dibromovinylphosphate), and by initial attack at the carbon atom of the C=O group, which is accompanied by the elimination of isobutylene to form an α-hydroxyphosphonate. © 1990 Plenum Publishing Corporation.
dc.relation.ispartofseries	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
dc.title	Reaction of 2-tert-butoxy-4,5-benzo-1,3,2-dioxaphospholane with tribromoacetaldehyde
dc.type	Article
dc.relation.ispartofseries-issue	8
dc.relation.ispartofseries-volume	38
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1755
dc.source.id	SCOPUS05685230-1989-38-8-SID34249967360

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