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 |
|