20292-14-2Relevant academic research and scientific papers
Polyelectrolyte-catalyzed Diels–Alder reactions
Pothanagandhi, Nellepalli,Sivaramakrishna, Akella,Vijayakrishna, Kari
, p. 132 - 136 (2016)
Imidazolium-based poly(ionic liquids) bearing bromide and bis(trifluoromethane)sulfonimide as counteranions [poly(ViEIm)Br and poly(ViEIm)NTf2] derived from reversible addition fragmentation chain transfer (RAFT) polymerization techniques are u
[AlCl3 + 2THF]: A new and efficient catalytic system for Diels-Alder cycloaddition of α,β-unsaturated carbonyl compounds under solvent-free conditions
Fringuelli, Francesco,Girotti, Rugiada,Pizzo, Ferdinando,Vaccaro, Luigi
, p. 2487 - 2489 (2007/10/03)
[AlCl3 + 2THF] is a new catalytic system for the Diels-Alder cycloaddition under SFC and air atmosphere. By using equimolar amounts of reactants, this catalyst prevents the polymerization of the diene and allows the corresponding adducts to be isolated with high regio- and stereocontrol and in excellent yields.
PALLADIUM DICHLORIDE-PROMOTED CYCLIZATIONS OF 1,5-DIENES. A NEW METHOD FOR FORMING CYCLOHEXENES.
Overman, Larry E.,Renaldo, Alfred F.
, p. 2235 - 2238 (2007/10/02)
1,5-Hexadienes, which are substituted with electron-withdrawing groups at carbon-3, undergo regioselective rearrangement to cyclohexenes upon treatment with palladium dichloride.
