65865-00-1Relevant academic research and scientific papers
Palladium-Catalyzed Hydrocarbonylative Cyclization of 1,5-Dienes
Zou, Suchen,Gao, Bao,Huang, Yao,Zhang, Tianze,Huang, Hanmin
, p. 6333 - 6336 (2019/08/26)
A novel and atom-economic palladium-catalyzed isomerization-hydrocarbonylative cyclization reaction of 1,5-dienes to 2-alkylidenecyclopentanones has been developed, which provides a rapid and straightforward approach to 2-alkylidenecyclopentanones with high stereoselectivity. The reaction was found to proceed via alkene isomerization and selective hydrocarbonylative cyclization to generate 2-alkylidenecyclopentanones with high selectivity.
Incorporation of 2-arylhexa-1,5-diene into pentasil zeolite: A distorted 1-arylcyclohexane-l,4-diyl radical cation at room temperature
Ikeda, Hiroshi,Minegishi, Tomonori,Miyashi, Tsutomu,Lakkaraju, Prasad S.,Sauers, Ronald R.,Roth, Heinz D.
, p. 2504 - 2511 (2007/10/03)
Incorporation into a redox-active pentasil zeolite [(Na,H)-ZSM-5] converted 2-arylhexa-1,5-dienes (9a-c; aryl = phenyl, tolyl, anisyl) into 1-arylcyclohexane-1,4-diyl radical cations, 10a-cì?+. The ESR spectra of 10a-cì?+ (six lines,
