Pregled bibliografske jedinice broj: 1057792
Unexpected reactivity of propiolic acid and triazoles
Unexpected reactivity of propiolic acid and triazoles // Knjiga sažetaka / Dejanović, Igor ; Vrsaljko, Domagoj ; Žižek, Krunoslav (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2020. str. 54-54 (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1057792 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Unexpected reactivity of propiolic acid and
triazoles
Autori
Gojšić, Tomislav ; Opačak, Saša ; Perić, Berislav ; Kirin, Srećko I.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Knjiga sažetaka
/ Dejanović, Igor ; Vrsaljko, Domagoj ; Žižek, Krunoslav - Zagreb : Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2020, 54-54
ISBN
978-953-6894-71-0
Skup
XIII. susret mladih kemijskih inženjera (SMLKI 2020)
Mjesto i datum
Zagreb, Hrvatska, 20.02.2020. - 21.02.2020
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
triazoles ; NMR spectroscopy ; X-ray crystallography
Sažetak
Peptide coupling reactions are one of the most well-known and ubiquitous reactions in chemical synthesis. Among the more common reagents used for amide bond formation are triazole compounds, such as the TBTU/HOBT couple, HATU and others. Propiolic acid is the simplest alkyne carboxylic acid and presents a logical choice for modification of pseudo peptide NH groups for pericyclic click reactions with azides. Continuing our work on pseudo peptide we have aimed to prepare their click analogues. However, we have observed unexpected reactivity of propiolic acid in mild conditions of peptide bond formation (DCM, DIPEA, R.T.). In the performed reactions unusual products were isolated which were identified and characterised using spectroscopic methods (NMR, IR), x-ray crystallography and mass spectrometry. Reactions were conducted using different ratios of HOBT and TBTU, and both N- addition and O-addition of triazolic reagents to triple bond were observed. N-addition occurred in tandem with peptide coupling when unprotected propiolic acid was used ; while in reactions with the ester of propiolic acid O- addition was observed. In these reactions both Z- and E-isomers were isolated. Structurally different products, formed by double addition of propiolic acid or its ester, were also isolated in some of the reactions. The goal of this research is to determine the scope of reactions of propiolic acid and triazole compounds and optimise reaction conditions in order to develop synthetically valuable reactions.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
IP-2014-09-1461 - Minimalni umjetni enzimi: Proširenje primjene posredne indukcije na nove supstrate i nove asimetrične reakcije (MArtEn) (Kirin, Srećko, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb