Pregled bibliografske jedinice broj: 82331
1, 3-Dipolar Cycloadditions to Polycyclic Aromatic Hydrocarbons
1, 3-Dipolar Cycloadditions to Polycyclic Aromatic Hydrocarbons // The third Brisbane biological and organic chemistry symposium (BBOCS-3)- Book of abstracts
Brisbane: Queensland University of Technology, 2002. (predavanje, međunarodna recenzija, sažetak, znanstveni)
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Naslov
1, 3-Dipolar Cycloadditions to Polycyclic Aromatic Hydrocarbons
Autori
Margetić, Davor ; Warrener, Ronald N. ; Butler, Douglas N.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
The third Brisbane biological and organic chemistry symposium (BBOCS-3)- Book of abstracts
/ - Brisbane : Queensland University of Technology, 2002
Skup
The third Brisbane biological and organic chemistry symposium (BBOCS-3)
Mjesto i datum
Brisbane, Australija, 29.11.2002
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
dipolar cycloadditions; aromatic hydrocarbons
Sažetak
The results of a 1, 3-dipolar cycloaddition reaction involving polyaromatic hydrocarbons (PAHs) as the dipolarophiles and the 1, 3-dipole formed by the ring-opening of a 5-oxabicyclo[2.1.0]pentane are reported. PAHs such as naphthalene, anthracene, benzanthracene, acenaphthene, phenanthrene, 9, 10-phenanthroline, gave mixtures of endo- (major) and exo- adducts, while fluorenone and anthraquinone yielded adducts across the carbonyl double bond. Only rare examples of cycloaddition reactions where anthracene acts as a dipolarophile are reported in literature
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA