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Pregled bibliografske jedinice broj: 71879

Photochemical Reactivity of N-substituted-2-styrylpyrrole


Basarić, Nikola; Marinić, Željko; Šindler-Kulyk, Marija
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)


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
Cavtat (Dubrovnik), Hrvatska, 01-06.09.2001

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


Projekt / tema
00981010
125004

Ustanove
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb