dc.contributor.author |
Arbuzov B. |
|
dc.contributor.author |
Erastov O. |
|
dc.contributor.author |
Remizov A. |
|
dc.contributor.author |
Ignat'eva S. |
|
dc.date.accessioned |
2018-09-14T20:24:06Z |
|
dc.date.available |
2018-09-14T20:24:06Z |
|
dc.date.issued |
1969 |
|
dc.identifier.issn |
0568-5230 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/132433 |
|
dc.description.abstract |
1. The five-membered chelate ring of enols of α-diketones and the six-membered chelate ring of β-cyanoketones, if it is formed, has a strength analogous to the intermolecular hydrogen bond. 2. A decrease in the conjugation in the quasiaromatic six-membered chelate ring of cyclic β-keto-esters with substituted five-membered rings is observed. © 1969 Consultants Bureau. |
|
dc.relation.ispartofseries |
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
|
dc.title |
The IR and UV spectra of enol forms of N-butyl-4-cyano-2, 3-dioxopyrrolidine and N-butyl-4-carboethoxy-2, 3-dioxopyrrolidine |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
4 |
|
dc.relation.ispartofseries-volume |
18 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
694 |
|
dc.source.id |
SCOPUS05685230-1969-18-4-SID34250492659 |
|