Pregled bibliografske jedinice broj: 523503
Methoxymethyl (MOM) group nitrogen protection of pyrimidines bearing C-6 acyclic side-chains
Methoxymethyl (MOM) group nitrogen protection of pyrimidines bearing C-6 acyclic side-chains // Molecules, 16 (2011), 6; 5113-5129 doi:10.3390/molecules16065113 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 523503 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Methoxymethyl (MOM) group nitrogen protection of pyrimidines bearing C-6 acyclic side-chains
Autori
Gazivoda Kraljević, Tatjana ; Petrović, Martina ; Krištafor, Svjetlana ; Makuc, Damjan ; Plavec, Janez ; Ross, Tobias L. ; Ametamey, Simon M. ; Raić-Malić, Silvana
Izvornik
Molecules (1420-3049) 16
(2011), 6;
5113-5129
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
N-methoxymethyl protecting group ; C-6 isobutyl pyrimidine derivatives ; N-1 and N-3 regioisomers ; NOE experiments ; positron emission tomography (PET)
Sažetak
Novel N-methoxymethylated (MOM) pyrimidine (4−13) and pyrimidine-2, 4-diones (15−17) nucleoside mimetics in which an isobutyl side-chain is attached at the C-6 position of the pyrimidine moiety were synthesized. Synthetic methods via O-persilylated or N-anionic uracil derivatives have been evaluated for the synthesis of N-1- and/or N-3-MOM pyrimidine derivatives with C-6 acyclic side-chains. A synthetic approach using an activated N-anionic pyrimidine derivative afforded the desired N, N-1, 3-diMOM and N-1-MOM pyrimidines 4 and 5 in good yield. Introduction of fluorine into the side-chain was performed with DAST as the fluorinating reagent to give a N, N-1, 3-diMOM pyrimidine 13 with a 1-fluoro-3-hydroxyisobutyl moiety at C-6. Conformational study of the monotritylated N-1-MOM pyrimidine 12 by the use of the NOE experiments revealed the predominant conformation of the compound to be one where the hydroxymethyl group in the C-6 side-chain is close to the N-1-MOM moiety, while the OMTr is in proximity to the CH3-5 group. Contrary to this no NOE enhancements between the N-1-MOM group and hydroxymethyl or fluoromethyl protons in 13 were observed, which suggested a nonrestricted rotation along the C-6 side-chain. Fluorinated N, N-1, 3-diMOM pyrimidine 13 emerged as a model compound for development of tracer molecules for non-invasive imaging of gene expression using positron emission tomography (PET).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-125-0982464-2925 - Razvoj i primjena novih molekula u pozitron-emisijskoj tomografiji (PET) (Raić-Malić, Silvana, MZOS ) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)
- EMBASE (Excerpta Medica)