Pregled bibliografske jedinice broj: 242180
Photochemically induced intramolecular reactions of the new stilbenyl-sydnones
Photochemically induced intramolecular reactions of the new stilbenyl-sydnones // "Central European Conference on Photochemistry" Book of Abstracts
Bad Hofgastein, 2006. str. 61-61 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 242180 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Photochemically induced intramolecular reactions of the new stilbenyl-sydnones
Autori
Butković, Kristina ; Basarić, Nikola ; Penić, Josip ; Šindler-Kulyk, Marija
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
"Central European Conference on Photochemistry" Book of Abstracts
/ - Bad Hofgastein, 2006, 61-61
Skup
CECP 2006 "Central European Conference on Photochemistry"
Mjesto i datum
Bad Hofgastein, Austrija, 05.03.2006. - 09.03.2006
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
sydnones; nitrile imines; 1; 7-electrocyclization; intramolecular reactions; photochemistry; laser flash photolysis; quinoline; benzodiazepine
Sažetak
In continuation of our work on photochemical methodology to polyheterocyclic compounds [1] by intramolecular cyclization reactions, the new stilbenyl-sydnones 1-3 are prepared [2]. It is known that 3, 4-disubstituted sydnones undergo photochemical ring opening [3] to nitrile imines, which can be trapped by various dipolarophiles giving corresponding cycloadducts. In this work the photolysis of the stilbenyl-sydnones give quinoline- (4) and benzodiazepine derivatives (5). This is the first example of 1, 7-electrocyclization of nitrile imines generated photochemically. The reaction mechanisms and LFP experiments will be discussed.
Izvorni jezik
Engleski
Znanstvena područja
Kemija