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dc.contributor.author | Arbuzov B. | |
dc.contributor.author | Kataev V. | |
dc.contributor.author | Arshinova R. | |
dc.contributor.author | Gubaidullin R. | |
dc.date.accessioned | 2018-09-20T20:41:31Z | |
dc.date.available | 2018-09-20T20:41:31Z | |
dc.date.issued | 1978 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/146181 | |
dc.description.abstract | 1. In solution, 5,5-bis(bromomethyl)-1,3,2-dioxaphosphorinane exists as an equilibrium mixture of conformera with trans-gauche and gauche-gauche orientations of the Br-C-C5-C-Br chain (the first index refers to the equatorial halomethyl group). 2. The 2-chloro- and 2-ethoxy-5,t-bis(chloromethyl)-1,3,2,-dioxaphosphorinanes exist not only in the trans-gauche and gauche-gauche forms but also in a gauche-trans form with the C-Cl bond of the axial chloromethyl group in trans orientation. 3. 2-Hydro-2-oxo-5,5-bis(halomethyl)-1,3,2-dioxaphosphorinanes exist as mixtures of conformers containing two chair forms with axial and equatorial phosphoryl groups. © 1979 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | The geometrical structures of phosphorus-containing heterocycles 20. 1,3,2-Dioxaphosphorinanes with two geminal axes of internal rotation | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 11 | |
dc.relation.ispartofseries-volume | 27 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 2179 | |
dc.source.id | SCOPUS05685230-1978-27-11-SID34250286699 |