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dc.contributor.author | Samitov Y. | |
dc.contributor.author | Zelikman Z. | |
dc.contributor.author | Shkrebets A. | |
dc.contributor.author | Kul'nevich V. | |
dc.date.accessioned | 2018-09-14T20:06:30Z | |
dc.date.available | 2018-09-14T20:06:30Z | |
dc.date.issued | 1974 | |
dc.identifier.issn | 0009-3122 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132134 | |
dc.description.abstract | The configuration and preferred conformations of a number of stereoisomeric 2-(α-furyl) 1,3-dioxanes were established by PMR spectroscopy. It is shown that cis orientation of the NO2 groups with respect to the furyl ring is primarily realized for 2-(α'-nitro-α-furyl)-5-ethyl-5-nitro-1,3-dioxanes. © 1975 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Chemistry of Heterocyclic Compounds | |
dc.title | Research on furan acetal compounds - VII. PMR spectra, configuration, and conformations of substituted 2-(α-furyl)-1,3-diozanes | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 3 | |
dc.relation.ispartofseries-volume | 10 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 276 | |
dc.source.id | SCOPUS00093122-1974-10-3-SID34250418334 |