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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 |