Takacs, James M. published the artcileCatalytic Palladium-Mediated Bisdiene Carbocyclizations: Bisdiene to Ene diene Cycloisomerizations, Synthetic Route of 4141-48-4, the publication is Journal of the American Chemical Society (1997), 119(25), 5804-5817, database is CAplus.
The palladium-catalyzed cycloisomerization of acyclic bisdienes to cyclized ene dienes defines a novel strategy for the stereoselective cyclization of certain unsym. bisdiene substrates to form functionalized five- and six-membered rings. The full details of our investigation into this novel cycloisomerization, including our observations on substrate requirements, stereoselectivity, the influence of the catalyst precursor, and some mechanistic insights drawn from deuterium labeling studies, are discussed.
Journal of the American Chemical Society published new progress about 4141-48-4. 4141-48-4 belongs to catalysis-chemistry, auxiliary class Aryl phosphine ligand,Mono-phosphine Ligands, name is Allyldiphenylphosphine oxide, and the molecular formula is C8H7ClO3, Synthetic Route of 4141-48-4.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia