20.500.12556/RUL-131194 Uporaba pirolon vsebujočih substratov v organokataliziranih reakcijah Application of pyrrolone involving substrates in organocatalysed reactions V sklopu magistrskega dela sem preučevala asimetrične pretvorbe derivatov pirolinona. Enantioselektivno sintezo sem dosegla z uporabo kiralnih nekovalentnih bifunkcionalnih organokatalizatorjev. Moje delo je obsegalo pripravo knjižnice racemnih produktov, s katerimi sem določila pogoje ločitve enantiomerov na kiralni HPLC koloni, ter enantiomerno obogatenih produktov, ki sem jim določila enantiomerni presežek. Sprva sem izvedla [4+2] anulacijo N-nesubstituiranih ariliden-Δ2-pirolin-4-onov z malononitrilom, rezultat katere so enantiomerno obogateni derivati dihidropirano[3,2-b]pirola. Pri določevanju enantiomernega presežka pretvorbe s kiralno HPLC kolono sem naletela na veliko dejavnikov, ki močno vplivajo na natančno določitev le-tega. V drugem delu sem kot izhodne substrate organokataliziranih pretvorb uporabila derivate tetramskih kislin. Z 1,4-adicijo tetramskih kislin na derivate trans-β-nitrostirena sem s tvorbo vezi C–C ustvarila kiralni center. Sintetizirala sem manjšo knjižnico aduktov tetramskih kislin in derivatov trans-β-nitrostirena, na katerih sem izvedla O-alkiliranje. Na izbrani neracemni N-Gly-Boc substituirani tetramski kislini sem izvedla serijo naknadnih pretvorb. S strategijo ortogonalne zaščite in peptidne kemije sem sintetizirala makrociklični produkt, ki vsebuje skelet pirolin-2-ona. In this master’s thesis, the research was focused on the application of pyrrolinone derivatives in asymmetric transformations. Enantioselective synthesis was achieved with the application of chiral noncovalent bifunctional organocatalysts. This work covers the preparation of a library of racemic compounds, that were used for the optimization of chiral HPLC method for the separation of enantiomers and subsequently for the determination of enantiomeric excess of the corresponding enantiomerically enriched compounds. In the first part, [4+2] annulation of N-unsubstituted arylidene-Δ2-pyrrolin-4-ones with malononitrile were examined, which resulted in nonracemic dihydropyrano[3,2-b]pyrrole derivatives. The determination of enantiomeric excess of chiral nonracemic compounds, done by chiral HPLC method, was accompanied with numerous factors, that must be put into the consideration, to be able to obtain accurate enantioselectivity results. In the following research, tetramic acids derivatives were applied in organocatalyzed reactions. 1,4-addition of tetramic acids to trans-β-nitrostyrene derivatives resulted in a chiral center formation as new C–C bond was formed. A small library of O-alkylated adducts of tetramic acids and trans-β-nitrostyrene derivatives was synthesized. A chiral nonracemic N-Gly-Boc substituted tetramic acid derivative was used for the selected follow-up modifications. With the implementation of orthogonal protection and peptide chemistry, macrocyclic product containing pyrrolin-2-one heterocycle was synthesized. asimetrična sinteza bifunkcionalna nekovalentna organokataliza pirolinonski derivati peptidna kemija makrociklizacija asymmetric synthesis bifunctional noncovalent organocatalysis pyrrolinone derivatives peptide chemistry macrocyclization true false false Slovenski jezik Angleški jezik Magistrsko delo/naloga 2021-09-23 13:20:07 2021-09-23 13:20:10 2022-09-10 04:10:32 0000-00-00 00:00:00 2021 0 0 0000-00-00 NiDoloceno NiDoloceno NiDoloceno 0000-00-00 0000-00-00 0000-00-00 17281 86460675 Gorenc_Ana_-_Uporaba_pirolon_vsebujocih_substratov_v_organokataliziranih_reakcijah.pdf Gorenc_Ana_-_Uporaba_pirolon_vsebujocih_substratov_v_organokataliziranih_reakcijah.pdf 1 B1E4115F034E3D635951A7AC6A0B1FAC 79e39c636e03a04a16cc063f7b72df278f2f407ccd54aeea4b207f25301a51b8 f1ec2bd8-1c5f-11ec-a523-00155dcfd717 https://repozitorij.uni-lj.si/Dokument.php?lang=slv&id=148465 Fakulteta za kemijo in kemijsko tehnologijo 0 0 0