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Pregled bibliografske jedinice broj: 764728

Ferrocenoyl-Substituted Pyrimidine Nucleobases. Experimental and Computational Study of Regioselective Acylation of Uracil, Thymine, and 5-Fluorouracil


Lapić, Jasmina; Havaić, Valentina; Šakić, Davor; Sanković, Krešimir; Djaković, Senka; Vrček, Valerije
Ferrocenoyl-Substituted Pyrimidine Nucleobases. Experimental and Computational Study of Regioselective Acylation of Uracil, Thymine, and 5-Fluorouracil // European journal of organic chemistry, 2015 (2015), 24; 5424-5431 doi:10.1002/ejoc.201500647 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 764728 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Ferrocenoyl-Substituted Pyrimidine Nucleobases. Experimental and Computational Study of Regioselective Acylation of Uracil, Thymine, and 5-Fluorouracil

Autori
Lapić, Jasmina ; Havaić, Valentina ; Šakić, Davor ; Sanković, Krešimir ; Djaković, Senka ; Vrček, Valerije

Izvornik
European journal of organic chemistry (1434-193X) 2015 (2015), 24; 5424-5431

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Acylation; Density functional calculations; Nucleobases; Reaction mechanisms; Regioselectivity

Sažetak
Uracil, thymine, and 5-fluorouracil (5-FU) have been ferrocenoylated selectively at the N1-position. Deprotonated pyrimidine nucleobases, prepared by sodium hydride (NaH) in dimethylformamide (DMF), reacted with ferrocenoyl chloride (FcCOCl), or ferrocenoyl ethyl carbonate (FcCOOCOOEt), in DMF to obtain a single product. Regioselectivity of these reactions have been analyzed in detail using NMR spectroscopy and quantum chemical calculations. 1H and 19F NMR spectra of reaction mixtures, and 13C NMR and 2D NOESY spectra of products, confirm the formation of the N1-isomer only. The calculated energy barrier for acetylation at the N3-position is significantly higher (> 40 kJ/mol), which suggests that the analogous reaction at the N1-position is kinetically controlled. The nucleophilic addition of pyrimidine bases to the carbonyl group of FcCOCl proceeds by a concerted SN2-like mechanism with the absence of the generally assumed tetrahedral intermediate.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove
Farmaceutsko-biokemijski fakultet, Zagreb,
Prehrambeno-biotehnološki fakultet, Zagreb

Citiraj ovu publikaciju

Lapić, Jasmina; Havaić, Valentina; Šakić, Davor; Sanković, Krešimir; Djaković, Senka; Vrček, Valerije
Ferrocenoyl-Substituted Pyrimidine Nucleobases. Experimental and Computational Study of Regioselective Acylation of Uracil, Thymine, and 5-Fluorouracil // European journal of organic chemistry, 2015 (2015), 24; 5424-5431 doi:10.1002/ejoc.201500647 (međunarodna recenzija, članak, znanstveni)
Lapić, J., Havaić, V., Šakić, D., Sanković, K., Djaković, S. & Vrček, V. (2015) Ferrocenoyl-Substituted Pyrimidine Nucleobases. Experimental and Computational Study of Regioselective Acylation of Uracil, Thymine, and 5-Fluorouracil. European journal of organic chemistry, 2015 (24), 5424-5431 doi:10.1002/ejoc.201500647.
@article{article, year = {2015}, pages = {5424-5431}, DOI = {10.1002/ejoc.201500647}, keywords = {Acylation, Density functional calculations, Nucleobases, Reaction mechanisms, Regioselectivity}, journal = {European journal of organic chemistry}, doi = {10.1002/ejoc.201500647}, volume = {2015}, number = {24}, issn = {1434-193X}, title = {Ferrocenoyl-Substituted Pyrimidine Nucleobases. Experimental and Computational Study of Regioselective Acylation of Uracil, Thymine, and 5-Fluorouracil}, keyword = {Acylation, Density functional calculations, Nucleobases, Reaction mechanisms, Regioselectivity} }

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


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