Влияние условий синтеза на образование пространственных изомеров диметилпроизводных гликолурила
| Parent link: | Перспективы развития фундаментальных наук=Prospects of Fundamental Sciences Development: сборник научных трудов XIII Международной конференции студентов, аспирантов и молодых ученых, г. Томск, 26-29 апреля 2016 г./ Национальный исследовательский Томский политехнический университет (ТПУ) ; под ред. И. А. Курзиной, Г. А. Вороновой.— , 2016 Т. 2 : Химия.— 2016.— [С. 244-246] |
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| Drugi avtorji: | , , |
| Izvleček: | Заглавие с титульного экрана Pharmacologic activity depends on spatial structures of substances, because there is specificity ofisomer action on biological target. Glycoluril derivatives have big range of biological activity. They are used astranquilizers. But methods of synthesis of dimethylglycoluril' isomers are contradictory in different literature.2,6-dimethylglycoluril and 2,4-dimethylglycoluril are produced by reaction between methylurea and glyoxal in different conditions. Using different solvent and acid catalysts we change ratio of isomers. |
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2016
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| Online dostop: | http://earchive.tpu.ru/handle/11683/25881 |
| Format: | Elektronski Book Chapter |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=618186 |
| Izvleček: | Заглавие с титульного экрана Pharmacologic activity depends on spatial structures of substances, because there is specificity ofisomer action on biological target. Glycoluril derivatives have big range of biological activity. They are used astranquilizers. But methods of synthesis of dimethylglycoluril' isomers are contradictory in different literature.2,6-dimethylglycoluril and 2,4-dimethylglycoluril are produced by reaction between methylurea and glyoxal in different conditions. Using different solvent and acid catalysts we change ratio of isomers. |
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