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 |
|