Pregled bibliografske jedinice broj: 683973
Functionalization of the benzobicyclo[3.2.1]octadiene skeleton via photocatalytic oxygenation of thiophene and furan derivatives: the impact of the type and position of the heteroatom
Functionalization of the benzobicyclo[3.2.1]octadiene skeleton via photocatalytic oxygenation of thiophene and furan derivatives: the impact of the type and position of the heteroatom // Journal of molecular structure, 1063 (2014), 83-91 doi:10.1016/j.molstruc.2014.01.055 (međunarodna recenzija, članak, znanstveni)
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Naslov
Functionalization of the benzobicyclo[3.2.1]octadiene skeleton via photocatalytic oxygenation of thiophene and furan derivatives: the impact of the type and position of the heteroatom
Autori
Vuk, Dragana ; Kikaš, Ilijana ; Molčanov, Krešimir ; Horváth, Ottó ; Škorić, Irena
Izvornik
Journal of molecular structure (0022-2860) 1063
(2014);
83-91
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
photocatalytic oxygenation ; porphyrins ; benzobicyclo[3.2.1]octadienes ; thiophene derivative ; furan derivative ; heteroatom impact
Sažetak
Photocatalytic oxygenations of a furan and two thiophene derivatives of benzobicyclo[3.2.1]octadiene have been realized by using anionic and cationic manganese(III) porphyrins as catalysts. The replace of oxygen with sulfur in the heteroaromatic ring considerably decreased the reactivity of these heterocyclic compounds, probably due to the increased aromaticity. The end-products of the oxygenation of the thiophene derivatives significantly deviated from most of those formed from the corresponding furan compounds ; the lower reactivity of the thiophene ring enhanced the role of the out-of-ring carbon atom in the reaction pathways. Besides, deviating from the behavior of the furan compounds, the types of the end-products formed from the corresponding thiophene derivatives did not depend on the charge of the photocatalyst, neither on the oxygen concentration. However, also in this case, the position of the heteroatom in the aromatic ring strongly affects the formation of the end- products.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-098-1191344-2943 - Protein-ligand međudjelovanja na atomnoj razini (Luić, Marija, MZOS ) ( CroRIS)
MZOS-125-0982933-2926 - Heteropolicikli, strukturne osnove za bioaktivne spojeve. Sinteza i fotokemija (Škorić, Irena, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
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
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)