1335234-46-2Relevant academic research and scientific papers
Thermal electrocyclization reactions II: Benzooctatetraenes and benzodecapentaenes
Vuk, Dragana,Marini?, ?eljko,Mol?anov, Kre?imir,Margeti?, Davor,?kori?, Irena
, p. 886 - 891 (2014/01/23)
Thermal electrocyclization reactions of benzooctatetraenes and benzodecapentaenes substituted with R=H, Cl, and methyl were studied experimentally and computationally. Methyl and unsubstituted benzooctatetraenes and benzodecapentaenes give the [4.2.0]bicyclooctadiene products by 8π,6π-electrocyclization. Chlorine substitution led to thermal rearrangement of the initially formed 8π,6π-electrocyclization intermediates to give unprecedented products.
Synthesis, photochemistry, and photophysics of butadiene derivatives: Influence of the methyl group on the molecular structure and photoinduced behavior
Skoric, Irena,Kikas, Ilijana,Kovacs, Margit,Fodor, Lajos,Marinic, Zeljko,Molcanov, Kresimir,Kojic-Prodic, Biserka,Horvath, Otto
experimental part, p. 8641 - 8657 (2011/12/15)
Novel butadiene derivatives display diverse photochemistry and photophysics. Excitation of 2-methyl-1-(o-vinylphenyl)-4-phenylbutadiene leads to the dihydronaphthalene derivative, whereas photolysis of the corresponding model o-methyl analogue results in
