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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 |