Pregled bibliografske jedinice broj: 427462
2, 8-Dithia-Dibenzo[e, h]Azulenes and Their 8-Oxa Analogs. Synthesis and Anti-Inflamatory Activity
2, 8-Dithia-Dibenzo[e, h]Azulenes and Their 8-Oxa Analogs. Synthesis and Anti-Inflamatory Activity // Heterocycles, 78 (2009), 10; 2489-2507 (međunarodna recenzija, članak, znanstveni)
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Naslov
2, 8-Dithia-Dibenzo[e, h]Azulenes and Their 8-Oxa Analogs. Synthesis and Anti-Inflamatory Activity
Autori
Ozimec Landek, Ivana ; Pešić, Dijana ; Novak, Predrag ; Stanić, Barbara ; Nujić, Krunoslav ; Merćep, Mladen ; Mesić, Milan
Izvornik
Heterocycles (0385-5414) 78
(2009), 10;
2489-2507
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
2; 8-dithia-dibenzo[e; h]azulenes; Synthesis; Activity; NMR
Sažetak
Synthesis of 2, 8-dithia-dibenzo[e, h]azulenes (III, X = S) and their 8-oxa analogs (III, X = O), 1 two novel classes of fused heterocyclic compounds, is described. Starting 11H-dibenzo[b, f]thiepin-10-one, 11H-dibenzo[b, f]oxepin- 10-one and its 2-chloro derivative (1a-c) were oxidized to 1, 2-diketones (2a-c) which subsequently reacted with 2, 2’ -dimethyl thiodiglycolate to form fused thiophene ring by Hinsberg cyclization reaction. Substituents at positions C(1) and C(3) were then further transformed in order to obtain aminoalkoxy derivatives 8-11. Structures of regioisomers 6c and 6d were elucidated using two-dimensional NMR techniques. All compounds with tetracyclic skeleton were tested in vitro for their anti-inflammatory activity.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
119-1191342-1083 - Interakcije i dizajn bioaktivnih molekula (Novak, Predrag, MZOS ) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Predrag Novak
(autor)
Krunoslav Nujić
(autor)
Ivana Ozimec Landek
(autor)
Mladen Merćep
(autor)
Dijana Pešić
(autor)
Milan Mesić
(autor)
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