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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 |