Pregled bibliografske jedinice broj: 13972
Photochemistry of beta-(condensed 2-furyl)-o-divinylbenzenes ; the influence of annelation on the reaction course
Photochemistry of beta-(condensed 2-furyl)-o-divinylbenzenes ; the influence of annelation on the reaction course // Book of Abstracts, 17th IUPAC Symposium on Photochemistry / unknown (ur.).
Barcelona: unknown, 1998. str. PA119-PA119 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 13972 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Photochemistry of beta-(condensed 2-furyl)-o-divinylbenzenes ; the influence of annelation on the reaction course
Autori
Vujković Cvijin, Irena ; Marinić, Željko ; Šindler-Kulyk, Marija
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts, 17th IUPAC Symposium on Photochemistry
/ Unknown - Barcelona : Unknown, 1998, PA119-PA119
Skup
17th IUPAC Symposium on Photochemistry
Mjesto i datum
Barcelona, Španjolska, 19.07.1998. - 24.07.1998
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
photochemistry; heteroaryl substituted o-divinylbenzene; beta-(2-furyl)-o-divinylbenzene; beta-(2-benzofuryl)-o-divinylbenzene; beta-naphthofuryl-o-divinylbenzene
Sažetak
As an extension of our interest in the photochemical behavior of heteroaryl-substituted o-divinylbenzenes, we investigated the photochemistry of annelated furan derivatives. While beta-(2-furyl)- and beta-(2-benzofuryl)-o-divinylbenzene undergo intramolecular cycloaddition to bicyclo[3.2.1]octadiene derivatives, beta-naphthofuryl-o-divinylbenzenes give, besides cis-trans-isomerization, only traces of dimeric products. Cyclization products are formed in all experiments. The structure determination of the products as well as the mechanism of the reaction are discussed.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
