174834-48-1Relevant articles and documents
Diastereoselective single oxygen ene reaction (Schenck reaction) and diastereoselective epoxidations of heteroatom-substituted acyclic chiral olefins: A mechanistic comparison
Adam,Brunker,Kumar,Peters,Peters,Schneider,Von Schnering
, p. 1899 - 1905 (1996)
The directing propensity of allylic and homoallylic heteroatom substituents on the diastereoselective singlet oxygen ene reaction (Schenck reaction) of acyclic, chiral olefins has been investigated. These extensive stereochemical results offer evidence fo
Photooxygenation of olefins, phenol, and sulfide using fullerodendrimer as catalyst
Takaguchi, Yutaka,Yanagimoto, Yasushi,Fujima, Shohoko,Tsuboi, Sadao
, p. 1142 - 1143 (2007/10/03)
Fullerodendrimer acts as a new catalyst that uses oxygen and light to generate singlet oxygen (1O2)- The dendrimer facilitates various types of singlet oxygenation reactions including ene reaction, the Diels-Alder reaction, and oxidation of phenol and sulfide.