Sinteza propargilnih epoksida i njihova rezolucija halogenhidrin-dehalogenazama
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| Title: | Sinteza propargilnih epoksida i njihova rezolucija halogenhidrin-dehalogenazama |
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| Authors: | Kolman, Robert Junior |
| Contributors: | Dokli, Irena, Primožič, Ines, Tomić, Antonija, Škalamera, Đani |
| Publisher Information: | Sveučilište u Zagrebu. Prirodoslovno-matematički fakultet. Kemijski odsjek., 2024. |
| Publication Year: | 2024 |
| Subject Terms: | propargil-alkoholi, biokataliza, biocatalysis, cinkom katalizirana Grignardova reakcija, halogenhidrin-dehalogenaze, PRIRODNE ZNANOSTI. Kemija, NATURAL SCIENCES. Chemistry, triazoli, propargylic alcohols, propargil-epoksidi, zinc-catalyzed Grignard reaction, kinetička rezolucija, halohydrin dehalogenases, kinetic resolution, Kemija. Kristalografija. Mineralogija, propargylic epoxides, triazoles, Chemistry. Crystallography. Mineralogy |
| Description: | Due to the presence of a carbon-carbon triple bond, propargylic epoxides are valuable building blocks in organic synthesis. However, known methods for their synthesis are scarce. Halohydrin dehalogenases (HHDH) are enzymes that facilitate the conversion of epoxides and halohydrins in both directions. Within this dissertation, two series of racemic terminal propargylic epoxides were synthesized. The number, position and type of substituents was varied. The use of propargylic epoxides as substrates in kinetic resolution reactions catalyzed by HHDHs was investigated. It was demonstrated that the aromatic monosubstituted and disubstituted compounds are good substrates, whereas the aliphatic monosubsituted compounds are not. The best performing aromatic monosubstituted and disubstituted compounds were used for synthesis of optically pure propargylic azido alcohols on a preparative scale. Optically pure compounds were then transformed in post-modification reactions. A compound containing the dihydrofuranyl triazole motif, found in compounds with known biological activities, was obtained. Raznovrsna reaktivnost uslijed prisustva ugljik-ugljik trostruke veze čini propargil-epokside vrijednim građevnim blokovima u organskoj sintezi. Međutim, postoji malo opisanih metoda za njihovu pripravu. Halogenhidrin-dehalogenaze (HHDH) su enzimi koji kataliziraju pretvorbu halogenhidrina i epoksida u oba smjera. U okviru ove doktorske disertacije sintetizirane su dvije serije racemičnih terminalnih propargil-epoksida. Spojevi su sintetizirani s različitim brojem, položajem i vrstom supstituenata. Time je istražena mogućnost upotrebe propargil-epoksida kao supstrata HHDH u reakcijama kinetičke rezolucije. Pokazano je da su aromatima monosupstituirani te disupstituirani spojevi dobri supstrati, dok alifatima monosupstituirani nisu. Najbolji supstrati iz skupine aromatskih te disupstituiranih spojeva upotrijebljeni su za sintezu optički čistih propargilnih azidoalkohola na preparativnoj skali. Na optički čistim spojevima provedene su reakcije postmodifikacija te je dobiven spoj koji sadrži dihidrofuranil-triazolni motiv koji se nalazi u spojevima s poznatim biološkim aktivnostima. |
| Document Type: | Doctoral thesis |
| File Description: | application/pdf |
| Access URL: | https://urn.nsk.hr/urn:nbn:hr:217:367925 https://repozitorij.pmf.unizg.hr/islandora/object/pmf:13934 https://urn.nsk.hr/urn:nbn:hr:217:367925 https://repozitorij.pmf.unizg.hr/islandora/object/pmf:13934/datastream/PDF |
| Rights: | URL: http://rightsstatements.org/vocab/InC/1.0/ |
| Accession Number: | edsair.dedup.wf.002..3df97ecde9f5d58b76b1b3a3d45e877c |
| Database: | OpenAIRE |
Nájsť tento článok vo Web of Science | Abstract: | Due to the presence of a carbon-carbon triple bond, propargylic epoxides are valuable building blocks in organic synthesis. However, known methods for their synthesis are scarce. Halohydrin dehalogenases (HHDH) are enzymes that facilitate the conversion of epoxides and halohydrins in both directions. Within this dissertation, two series of racemic terminal propargylic epoxides were synthesized. The number, position and type of substituents was varied. The use of propargylic epoxides as substrates in kinetic resolution reactions catalyzed by HHDHs was investigated. It was demonstrated that the aromatic monosubstituted and disubstituted compounds are good substrates, whereas the aliphatic monosubsituted compounds are not. The best performing aromatic monosubstituted and disubstituted compounds were used for synthesis of optically pure propargylic azido alcohols on a preparative scale. Optically pure compounds were then transformed in post-modification reactions. A compound containing the dihydrofuranyl triazole motif, found in compounds with known biological activities, was obtained.<br />Raznovrsna reaktivnost uslijed prisustva ugljik-ugljik trostruke veze čini propargil-epokside vrijednim građevnim blokovima u organskoj sintezi. Međutim, postoji malo opisanih metoda za njihovu pripravu. Halogenhidrin-dehalogenaze (HHDH) su enzimi koji kataliziraju pretvorbu halogenhidrina i epoksida u oba smjera. U okviru ove doktorske disertacije sintetizirane su dvije serije racemičnih terminalnih propargil-epoksida. Spojevi su sintetizirani s različitim brojem, položajem i vrstom supstituenata. Time je istražena mogućnost upotrebe propargil-epoksida kao supstrata HHDH u reakcijama kinetičke rezolucije. Pokazano je da su aromatima monosupstituirani te disupstituirani spojevi dobri supstrati, dok alifatima monosupstituirani nisu. Najbolji supstrati iz skupine aromatskih te disupstituiranih spojeva upotrijebljeni su za sintezu optički čistih propargilnih azidoalkohola na preparativnoj skali. Na optički čistim spojevima provedene su reakcije postmodifikacija te je dobiven spoj koji sadrži dihidrofuranil-triazolni motiv koji se nalazi u spojevima s poznatim biološkim aktivnostima. |
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