6938-63-2Relevant academic research and scientific papers
Cerium-catalyzed, aerobic oxidative synthesis of 1,2-dioxane derivatives from styrene and their fragmentation into 1,4-dicarbonyl compounds
Roessle, Michael,Werner, Thomas,Frey, Wolfgang,Christoffers, Jens
, p. 5031 - 5038 (2007/10/03)
1,4-Diketones were prepared by cerium-catalyzed oxidative coupling of styrene with molecular oxygen and 1,3-dicarbonyl compounds. This two-step sequence was performed as a one-pot procedure without isolation of the intermediate products. The first step is
PHOTOCHEMISTRY OF SUBSTITUTED CYCLIC ENONES. PART 6. PHOTOCHEMICAL REACTIONS OF 5-ARYLMETHYL-3-PHENYLCYCLOPENT-2-ENONES. A PHOTOSTATIONARY STATE1,2
Clements, Michael T.,McMurry, Brian H.
, p. 1810 - 1813 (2007/10/02)
Photolysis of 5-(1-and 2-naphtylmethyl)-3-phenylcyclopent-2-enones affords cycloaddition products, the 7,8- and 5,6-benzo-fused 10-phenyltetracyclo3,10.04,9>dodeca-5,7-dien-2-ones respectively, in equilibrium with the
