dc.contributor.advisor |
Kafka, Stanislav
|
|
dc.contributor.author |
Karteczková, Adéla
|
|
dc.date.accessioned |
2023-12-20T13:25:09Z |
|
dc.date.available |
2023-12-20T13:25:09Z |
|
dc.date.issued |
2022-12-31 |
|
dc.identifier |
Elektronický archiv Knihovny UTB |
|
dc.identifier.uri |
http://hdl.handle.net/10563/53845
|
|
dc.description.abstract |
Kondenzací bis(2,4,6-trichlorfenyl)esterů substituované kyseliny malonové s anily methylketonů přpravenými eliminací kyanovodíku z odpovídajících -aminonitrilů, byly připraveny čtyři deriváty 4-hydroxypyridin-2(1H)-onu. Dva z nich byly reakcí se sulfurylchloridem převedeny na odpovídající 3,5-dichlorpyridin-2,4(1H,3H)-diony. Z jednoho 3,5-dichlorpyridin-2,4(1H,3H)-dionu byl reakcí s azidem sodným připraven 3 azido-5-chlorpyridin-2,4(1H,3H)-dion. |
|
dc.format |
47 s. (59 567 znaků) |
|
dc.language.iso |
cs |
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dc.publisher |
Univerzita Tomáše Bati ve Zlíně |
|
dc.rights |
Bez omezení |
|
dc.subject |
syntéza
|
cs |
dc.subject |
4-hydroxypyridin-2
|
cs |
dc.subject |
1H
|
cs |
dc.subject |
-on
|
cs |
dc.subject |
3
|
cs |
dc.subject |
5-dichlorpyridin-2
|
cs |
dc.subject |
4
|
cs |
dc.subject |
1H
|
cs |
dc.subject |
3H
|
cs |
dc.subject |
-dion
|
cs |
dc.subject |
3-azido-5-chlorpyridin-2
|
cs |
dc.subject |
4
|
cs |
dc.subject |
1H
|
cs |
dc.subject |
3H
|
cs |
dc.subject |
-dion
|
cs |
dc.subject |
synthesis
|
en |
dc.subject |
4 hydroxypyridine 2
|
en |
dc.subject |
1H
|
en |
dc.subject |
-one
|
en |
dc.subject |
3
|
en |
dc.subject |
5-dichloropyridine-2
|
en |
dc.subject |
4
|
en |
dc.subject |
1H
|
en |
dc.subject |
3H
|
en |
dc.subject |
-dione
|
en |
dc.subject |
3-azido-5-chloropyridine-2
|
en |
dc.subject |
4
|
en |
dc.subject |
1H
|
en |
dc.subject |
3H
|
en |
dc.subject |
-dione
|
en |
dc.title |
Reakce 4-hydroxypyridin-2-onů s halogenačními činidly a reakce získaných halogenderivátů s nukleofily |
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dc.title.alternative |
Reactions of 4-hydroxypyridin-2-ones with Halogenating Agents and Reactions of the Obtained Halogen Derivatives with Nucleophiles |
|
dc.type |
diplomová práce |
cs |
dc.contributor.referee |
Potáček, Milan |
|
dc.date.accepted |
2023-06-08 |
|
dc.description.abstract-translated |
By the condensation of bis(2,4,6-trichlorophenyl)esters of substitued malonic acids with methylketone aniles, which were prepared by elimination of hydrogen cyanide from the correspondning -aminonitriles, four derivates of 4 hydroxypyridine 2(1H)-one were synthetized. Two of them were then converted to corresponding 3,5-dichloropyridine-2,4(1H,3H)-diones by reaction with sulfuryl chloride. One of the 3,5-dichloropyridine-2,4(1H,3H)-diones was transformed to 3 azido 5 chloropyridine-2,4(1H,3H)-dione by reaction with sodium azide. |
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dc.description.department |
Ústav chemie |
|
dc.thesis.degree-discipline |
- |
cs |
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 potravin a bioaktivních látek |
cs |
dc.thesis.degree-program |
Chemistry of Food and Bioactive Compounds |
en |
dc.identifier.stag |
64606
|
|
dc.date.submitted |
2023-05-12 |
|