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dc.contributor.author | Arbuzov B. | |
dc.contributor.author | Butenko G. | |
dc.contributor.author | Vereshchagin A. | |
dc.contributor.author | Shishkina N. | |
dc.date.accessioned | 2018-09-14T20:29:08Z | |
dc.date.available | 2018-09-14T20:29:08Z | |
dc.date.issued | 1974 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132512 | |
dc.description.abstract | 1. The steric structure of adducts of dichloroketene and cyclohexene, dichloroketene and methyl-cyclohexene, dimethylketene and dihydropyran was investigated by the methods of dipole moments and molar Kerr constants. 2. For all the adducts, the preferential conformation of the bicyclo[4,2,0]octan-7-one system is the anti-boat conformation. 3. The adduct of dimethylketene and dihydropyran has the structure of 8,8-dimethyl-2-oxobicyclo-[4,2,0] octan-7-one. The formation of such a structure is apparently determined by the electron donor influence of the oxygen atom in dihydropyran on the process of cycloaddition. © 1974 Consultants Bureau. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | Investigation of the steric structure of certain compounds of the bicyclo-[4,2,0]octan-7-one series | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 2 | |
dc.relation.ispartofseries-volume | 23 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 285 | |
dc.source.id | SCOPUS05685230-1974-23-2-SID34250426006 |