Hirālu piridīna atvasinājumu katalizēta Steglich reakcija
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Latvijas Universitāte
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lav
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Hirālu piridīna atvasinājumu katalizēta Steglich reakcija. Elise Elza Vīgante, zinātniskais vadītājs asoc. prof. Artis Kinēns. Bakalaura darbs, 39 lappuses, 27 attēli, 1 tabula, 36 literatūras avoti, 2 pielikumi. Latviešu valodā. Darbā tika sintezēti hirālie katalizatori un no aminoskābēm atvasināti substrāti. Izmantojot 4-metoksipiridīna hirālo katalizatoru veica Steglich pārgrupēšanos un pētīja substrātu ietekmi uz reakcijas produkta enantiomēro pārākumu.
Steglich reaction catalysed by chiral pyridine derivatives. Elise Elza Vīgante, scientific supervisor Asoc. Prof. Artis Kinēns. Bachelor work, 39 pages, 27 figures, 1 table, 36 references, 1 appendix. In Latvian. In this work chiral catalysts and amino acid derived substrates were synthesised. Steglich rearrangements were carried out using 4-methoxypyridine chiral catalyst and the effect of the substrates on the enantiomeric superiority of the reaction product was studied.
Steglich reaction catalysed by chiral pyridine derivatives. Elise Elza Vīgante, scientific supervisor Asoc. Prof. Artis Kinēns. Bachelor work, 39 pages, 27 figures, 1 table, 36 references, 1 appendix. In Latvian. In this work chiral catalysts and amino acid derived substrates were synthesised. Steglich rearrangements were carried out using 4-methoxypyridine chiral catalyst and the effect of the substrates on the enantiomeric superiority of the reaction product was studied.