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dc.contributor.author | Arbuzov B. | |
dc.contributor.author | Sorokina T. | |
dc.contributor.author | Vinogradova V. | |
dc.date.accessioned | 2018-09-14T20:25:33Z | |
dc.date.available | 2018-09-14T20:25:33Z | |
dc.date.issued | 1971 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132463 | |
dc.description.abstract | 1. Trimethyl phosphite at -14° adds to 5-benzalbarbituric acid to give the (1:1) adduct with a bipolar structure, which then isomerizes to the methyl ester of the enol form of the dimethyl ester of barbituryl-5-benzylphosphonic acid. The latter is also formed by running the reaction at room temperature. 2. In the presence of glacial acetic acid, trimethyl phosphite reacts with 5-benzalbarbituric acid to give the dimethyl ester of barbituryl-5-benzylphosphonic acid in the enol form. 3. The reaction of tri(dimethylamino)phosphine with 5-benzalbarbituric acid gave the crystalline (1:1) adduct, which has the structure of a bipolar ion containing the P-C bond. © 1971 Consultants Bureau. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | Reaction of 5-benzalbarbituric acid with trimethyl phosphite and tri(dimethylamino) phosphine | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 3 | |
dc.relation.ispartofseries-volume | 20 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 506 | |
dc.source.id | SCOPUS05685230-1971-20-3-SID34250465185 |