An Intramolecular Substitution of Hydroperoxy-endoperoxide to a Bis-endoperoxide

Autor: (Horasan) Kishali, Nurhan, Sahin, Ertan, Kara, Yunus
Zdroj: Organic Letters; April 2006, Vol. 8 Issue: 9 p1791-1793, 3p
Abstrakt: A new and stereospecific synthesis for bis-endoperoxide has been developed starting from tetrahydronaphthalene. Photooxygenation of tetrahydronaphthalene resulted in the formation of hydroperoxy-endoperoxide. The bromination reaction of hydroperoxy-endoperoxide gave bis-endoperoxide, whose exact configuration has been determined by X-ray analysis. The lowest-energy conformer of bis-endoperoxide is the boat-chair form.
Databáze: Supplemental Index