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dc.contributor.author | Soboleva S. | |
dc.contributor.author | Gren' A. | |
dc.contributor.author | Samitov Y. | |
dc.contributor.author | Bogatskii A. | |
dc.date.accessioned | 2018-09-14T20:06:19Z | |
dc.date.available | 2018-09-14T20:06:19Z | |
dc.date.issued | 1972 | |
dc.identifier.issn | 0009-3122 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132130 | |
dc.description.abstract | The configurations and preferred conformations in series of 4,5-dialkyl and 4,5,5-trialkylsubstituted 2,2-dimethyl-1,3-dioxanes were studied. It was proved by PMR spectroscopy that the low-boiling isomers have the cis configuration, while the high-boiling isomers have the trans configuration; moreover, all of the isomers are found in the preferred chair conformation. This conformation experiences a certain amount of distortion, the degree of which depends on the number and character of the substituents in the 5 position. © 1974 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Chemistry of Heterocyclic Compounds | |
dc.title | Stereochemistry of heterocycles - XVII. Configuration and conformation of some stereoisomeric 4,5-substituted 2,2-dimethyl-1,3-dioxanes | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 11 | |
dc.relation.ispartofseries-volume | 8 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1321 | |
dc.source.id | SCOPUS00093122-1972-8-11-SID34250469915 |