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dc.contributor.author | Samitov Y. | |
dc.contributor.author | Yavorskii A. | |
dc.contributor.author | Gren' A. | |
dc.contributor.author | Bogat-skii A. | |
dc.contributor.author | Stepanova O. | |
dc.date.accessioned | 2018-09-14T20:06:48Z | |
dc.date.available | 2018-09-14T20:06:48Z | |
dc.date.issued | 1975 | |
dc.identifier.issn | 0009-3122 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132140 | |
dc.description.abstract | 2-Methyl-and 2,5-dialkyl-5-phenoxy-1,3-dioxanes were synthesized and separated into their geometrical isomers by precision rectification. The configuration and conformations of these isomers were determined by PMR spectroscopy. It is shown that the low-boiling trans isomers exist primarily in the chair conformation with an equatorial phenoxy group, whereas the high-boiling cis isomers exist primarily in the chair conformation with an axial phenoxy group. © 1976 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Chemistry of Heterocyclic Compounds | |
dc.title | Stereochemistry of heterocycles - XXXIX. Stereochemistry of 2-methyl-5-alkyl-5-phenoxy-1.3-dioxanes | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 8 | |
dc.relation.ispartofseries-volume | 11 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 904 | |
dc.source.id | SCOPUS00093122-1975-11-8-SID34250393178 |