dc.contributor.advisor |
Rudolf, Ondřej
|
|
dc.contributor.author |
Černoch, Zdeněk
|
|
dc.date.accessioned |
2015-03-08T21:03:44Z |
|
dc.date.available |
2015-03-08T21:03:44Z |
|
dc.date.issued |
2014-02-07 |
|
dc.identifier |
Elektronický archiv Knihovny UTB |
|
dc.identifier.uri |
http://hdl.handle.net/10563/28948
|
|
dc.description.abstract |
Práce se zaměřuje především na optimalizaci přípravy, samotnou přípravu a charakterizaci nových chinolin-2,4-dionů nesoucích v poloze 3 nitrilovou skupinu ze snadno dostupných 3-chlorchinolin-2,4-dionů, které jsou v poloze 1 buď nesubstituované nebo substituované arylem či alkylem. S takto připravenými nitrily byly provedeny pokusy s redukčními činidly. |
|
dc.format |
74 s. (88271 znaků) |
|
dc.language.iso |
cs |
|
dc.publisher |
Univerzita Tomáše Bati ve Zlíně |
|
dc.rights |
Bez omezení |
|
dc.subject |
chinolin-2
|
cs |
dc.subject |
4-dion
|
cs |
dc.subject |
nukleofilní substituce
|
cs |
dc.subject |
3-chlorchinolin-2
|
cs |
dc.subject |
4
|
cs |
dc.subject |
1H
|
cs |
dc.subject |
3H
|
cs |
dc.subject |
-dion
|
cs |
dc.subject |
karbonitril
|
cs |
dc.subject |
nitril
|
cs |
dc.subject |
kyanid sodný
|
cs |
dc.subject |
tetrahydridoboritan sodný
|
cs |
dc.subject |
redukce karbonylů
|
cs |
dc.subject |
quinoline
|
en |
dc.subject |
nucleophilic substitution
|
en |
dc.subject |
3-chlorquinoline-2
|
en |
dc.subject |
4
|
en |
dc.subject |
1H
|
en |
dc.subject |
3H
|
en |
dc.subject |
-diones
|
en |
dc.subject |
carbonitrile
|
en |
dc.subject |
nitrile
|
en |
dc.subject |
sodium cyanide
|
en |
dc.subject |
sodium tetrahydridoborate
|
en |
dc.subject |
reduction of carbonyles
|
en |
dc.title |
Studium přeměn 3-chlorchinolin-2,4-dionů na 2,4-dioxochinolin-3-karbonitrily |
|
dc.title.alternative |
Study of Conversions of 3-chlorquinoline-2,4-diones into 2,4-dioxoquinoline-3-carbonitriles |
|
dc.type |
diplomová práce |
cs |
dc.contributor.referee |
Klásek, Antonín |
|
dc.date.accepted |
2014-06-10 |
|
dc.description.abstract-translated |
The diploma thesis is focused on preparation, its optimalization and characterization of novel quinoline-2,4-diones bearing next to halogen nitrile group from easily accesible 3-chlorquinoline-2,4-diones which are in 1 unsubstituated or substituated by aryl/alkyl. Reductions were made with those compounds, aminomethylene group is expected on the other hand reduction of carbonyle group is also possible to give derivates of hydroxyquinolines. |
|
dc.description.department |
Ústav chemie |
|
dc.thesis.degree-discipline |
Chemie potravin a bioaktivních látek |
cs |
dc.thesis.degree-discipline |
Food Chemistry and Chemistry of Bioactive Substances |
en |
dc.thesis.degree-grantor |
Univerzita Tomáše Bati ve Zlíně. Fakulta technologická |
cs |
dc.thesis.degree-grantor |
Tomas Bata University in Zlín. Faculty of Technology |
en |
dc.thesis.degree-name |
Ing. |
|
dc.thesis.degree-program |
Chemie a technologie potravin |
cs |
dc.thesis.degree-program |
Chemistry and Food Technologies |
en |
dc.identifier.stag |
34746
|
|
utb.result.grade |
B |
|
dc.date.submitted |
2014-05-16 |
|