Показать сокращенную информацию
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 |