dc.contributor.author |
Arbuzov B. |
|
dc.contributor.author |
Isaeva Z. |
|
dc.contributor.author |
Andreeva I. |
|
dc.date.accessioned |
2018-09-14T20:23:06Z |
|
dc.date.available |
2018-09-14T20:23:06Z |
|
dc.date.issued |
1967 |
|
dc.identifier.issn |
0568-5230 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132413 |
|
dc.description.abstract |
1. Under the action of sodium methoxide in methanol 2,3-epoxypinane forms trans-2(10)-pinen-3-ol (mixture of l- and d l-forms) and 3-pinanone (mixture of d- and d l-forms). 2. Under the conditions of the reaction of 2,3-epoxypinane with methanol 3-pinanone may be formed in two ways: 1) mainly directly by the isomerization of the epoxide into the ketone, and 2) by the isomerization of the primary reaction product 2(10)-pinen-3-ol under the action of the base. © 1968 Consultants Bureau. |
|
dc.relation.ispartofseries |
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
|
dc.title |
Reaction of 2,3-epoxypinane with methanol in presence of sodium methoxide |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
6 |
|
dc.relation.ispartofseries-volume |
16 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1252 |
|
dc.source.id |
SCOPUS05685230-1967-16-6-SID34250537769 |
|