dc.contributor.author |
Pavelyev R. |
|
dc.contributor.author |
Gnevashev S. |
|
dc.contributor.author |
Vafina R. |
|
dc.contributor.author |
Gnezdilov O. |
|
dc.contributor.author |
Dobrynin A. |
|
dc.contributor.author |
Lisovskaya S. |
|
dc.contributor.author |
Nikitina L. |
|
dc.contributor.author |
Klimovitskii E. |
|
dc.date.accessioned |
2018-09-18T20:11:37Z |
|
dc.date.available |
2018-09-18T20:11:37Z |
|
dc.date.issued |
2012 |
|
dc.identifier.issn |
0959-9436 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/137443 |
|
dc.description.abstract |
Both exo- and endo-isomers of 4-phenyl-3,5,8-trioxabicyclo[5.1.0]octane were reacted with thiophenol to afford individual diastereomers of hydroxy sulfides which were further processed in search for new antimycotic substances. © 2012 Mendeleev Communications. All rights reserved. |
|
dc.relation.ispartofseries |
Mendeleev Communications |
|
dc.title |
Synthesis and antimycotic properties of hydroxy sulfides derived from exo- and endo-4-phenyl-3,5,8-trioxabicyclo[5.1.0]octanes |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
3 |
|
dc.relation.ispartofseries-volume |
22 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
127 |
|
dc.source.id |
SCOPUS09599436-2012-22-3-SID84861618609 |
|