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Sinteza derivatov L-arginina iz N-benziloksikarbonil-L-ornitina
ID Suhorepec, Nadja (Author), ID Svete, Jurij (Mentor) More about this mentor... This link opens in a new window

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Abstract
V sklopu diplomskega dela smo želeli pripraviti del tetrapeptidne elektrofilne sonde, in sicer Arg(Boc)2-SerOMe (4). Uspešno smo sintetizirali N-Cbz-Arg(Boc)2-OH (1) iz N-Cbz-Orn(Boc)-OH in N,N'-Boc2-S-metilizotiosečnine. Spojino 1 smo nato spojili s serin metil estrom hidrokloridom v dipeptid N-Cbz-Arg(Boc)2-SerOMe (2) v prisotnosti treh različnih aktivacijskih reagentov: CDI, EEDQ in EDC. Pri tem se je kot stranski produkt tvoril α-N-benziloksikarbonil-ω,ω'-di-N-t-butoksikarbonil-L-arginin laktam (3). Poskus zmanjšanja deleža spojine 3 je bil neuspešen. V zadnjem koraku sinteze spojine 4 smo spojini 2 selektivno odstranili Cbz zaščitno skupino s katalitskim hidrogeniranjem.

Language:Slovenian
Keywords:dipeptid, aktivacijski reagenti, zaščitna skupina, hidrogenoliza
Work type:Bachelor thesis/paper
Typology:2.11 - Undergraduate Thesis
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Year:2022
PID:20.500.12556/RUL-139157 This link opens in a new window
COBISS.SI-ID:122508291 This link opens in a new window
Publication date in RUL:31.08.2022
Views:692
Downloads:95
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Secondary language

Language:English
Title:Synthesis of derivatives of L-arginine from N-benzyloxycarbonyl-L-ornithine
Abstract:
As a part of my Bachelor's thesis we aimed to prepare a part of a tetrapeptide electrophilic probe, namely Arg(Boc)2-SerOMe (4). N-Cbz-Arg(Boc)2-OH (1) was successfully synthesized from N-Cbz-Orn(Boc)-OH and N,N'-Boc2-Smethylisothiourea. Compound 1 was then coupled with serine methyl ester hydrochloride to the dipeptide N-Cbz-Arg(Boc)2-SerOMe (2) in the presence of three different coupling reagents: CDI, EEDQ and EDC. α-N-benzyloxycarbonyl-ω,ω'-di-N-tbutoxycarbonyl-L-arginine lactam (3) was formed as a by-product. An attempt to reduce the proportion of compoud 3 was unsuccessful. As a last step in the synthesis of compound 4, Cbz protecting group was selectively removed from compound 2 by catalytic hydrogenation.

Keywords:dipeptide, coupling reagents, protecting group, hydrogenolysis

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