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dc.contributor.author | Arbuzov B. | |
dc.contributor.author | Aganov A. | |
dc.contributor.author | Klochkov V. | |
dc.contributor.author | Anonimova I. | |
dc.contributor.author | Chadaeva N. | |
dc.contributor.author | Lyubimtseva O. | |
dc.date.accessioned | 2018-09-14T20:44:11Z | |
dc.date.available | 2018-09-14T20:44:11Z | |
dc.date.issued | 1984 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132650 | |
dc.description.abstract | 1. 2-Chloro- and 2-bromo-5,6-benzo-1,3,2-dioxarsepines have the chair conformation with axial arrangement of the exocyclic bond at the arsenic atom. 2. In the case of 2-phenyl-, 2-(p-bromophenyl)-, and 2-(p-nitrophenyl)-5,6-benzo-1,3,2-dioxarsepines an equilibrium exists in solution between the chair-a and twist conformers, the ratio of which is close to unity.13C NMR spectra of "frozen conformers" at 143°K have been obtained for the first time for such a series of compounds. © 1985 Plenum Publishing Corporation. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | Stereochemistry of 2-substituted 5,6-benzo-1,3,2-dioxarsepines | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 8 | |
dc.relation.ispartofseries-volume | 33 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1627 | |
dc.source.id | SCOPUS05685230-1984-33-8-SID1942533192 |