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Preparation and structure of 2-acetyl-2,3-epoxycarane

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dc.contributor.author Ibragimova N.
dc.contributor.author Vul'fson S.
dc.contributor.author Donskova A.
dc.contributor.author Bikeev S.
dc.contributor.author Vereshchagin A.
dc.contributor.author Samitov Y.
dc.date.accessioned 2018-09-14T20:41:26Z
dc.date.available 2018-09-14T20:41:26Z
dc.date.issued 1982
dc.identifier.issn 0568-5230
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/132615
dc.description.abstract 1. 2-Acetyl-α-2,3-epoxycarane which exists in solution as a single gauche conformer with minimal polarity was synthesized by the epoxidation of 2-acetyl-2-carene by perphthalic acid. 2. The conjugation in the system of double bonds in 2-acetyl-2-carene is disturbed due to acoplanarity of the C=C-C=O fragment. © 1982 Plenum Publishing Corporation.
dc.relation.ispartofseries Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
dc.title Preparation and structure of 2-acetyl-2,3-epoxycarane
dc.type Article
dc.relation.ispartofseries-issue 2
dc.relation.ispartofseries-volume 31
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 317
dc.source.id SCOPUS05685230-1982-31-2-SID34250227319


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