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 |
|