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dc.contributor.author | Arbuzov B. | |
dc.contributor.author | Zoroastrova V. | |
dc.contributor.author | Neklesova I. | |
dc.contributor.author | Kudrina M. | |
dc.contributor.author | Egorova N. | |
dc.contributor.author | Tudrii G. | |
dc.date.accessioned | 2018-09-14T20:26:21Z | |
dc.date.available | 2018-09-14T20:26:21Z | |
dc.date.issued | 1972 | |
dc.identifier.issn | 0568-5230 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132478 | |
dc.description.abstract | 1. A series of derivatives of phosphorus acids and α-chloroallyl alcohol was obtained. 2. Increasing the length of the hydrocarbon radical attached to the phosphorus atom from C1 to C6 leads to a sharp increase in the selectivity of the action of the compounds toward Trichophyton gypseum and Epidermophyton Kaufmann-Wolf. A further increase in the length of the radical decreases the anti-fungal activity of the compounds. 3. It was established that di-n-amyl α-chloroallyl phosphate has the highest selectivity index of action toward dermatophytes. © 1972 Consultants Bureau. | |
dc.relation.ispartofseries | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science | |
dc.title | Derivatives of phosphorus acids and α-chloroallyl alcohol - Communication 2. Synthesis of mixed α-chloroallyl esters of phosphoric acid and some of their biological properties | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 5 | |
dc.relation.ispartofseries-volume | 21 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1106 | |
dc.source.id | SCOPUS05685230-1972-21-5-SID34250442608 |