Pregled bibliografske jedinice broj: 71879
Photochemical Reactivity of N-substituted-2-styrylpyrrole
Photochemical Reactivity of N-substituted-2-styrylpyrrole // 8th European Symposium on Organic Reactivity / Eckert-Maksić, M. (ur.).
Zagreb: Institut Ruđer Bošković, 2001. str. 188-188 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 71879 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Photochemical Reactivity of N-substituted-2-styrylpyrrole
Autori
Basarić, Nikola ; Marinić, Željko ; Šindler-Kulyk, Marija
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
8th European Symposium on Organic Reactivity
/ Eckert-Maksić, M. - Zagreb : Institut Ruđer Bošković, 2001, 188-188
Skup
8th European Symposium on Organic Reactivity
Mjesto i datum
Dubrovnik, Hrvatska; Cavtat, Hrvatska, 01.09.2001. - 06.09.2001
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
photochemistry; reactivity; pyrroles; bicyclo[3.2.1]octadiene
Sažetak
We have been interested in the synthesis and photochemical reactivity of o-vinylstilbenes as a method for the preparation of polycyclic compounds, potentially pharmacologically interesting substances. Whereas on irradiation of furan derivatives (1) the intramolecular cycloaddition takes place, resulting in the formation of the bicyclo[3.2.1]octadiene furan derivatives (3), the pyrrole derivatives (2) give the dimers (4), formed by the addition of one pyrrole ring to the double bond of the other molecule in a regiospecific way. In order to obtain the pyrrole-bicyclo[3.2.1]octadiene structure the nitrogen of the pyrrole ring is substituted with the electron withdrawing substituents. By irradiation of such substituted pyrrole derivatives of o-divinylbenzene desired photoproducts (6) are obtained.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb