66336-61-6Relevant academic research and scientific papers
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,
Synthesis of (+/-)-Mesembranol and (+/-)-O-Methyljoubertiamine. Aza-Ring Expansion of cis-Bicyclooctanones
Jeffs, Peter W.,Cortese, Nicholas A.,Wolfram, Joachim
, p. 3881 - 3886 (2007/10/02)
The Syntheses of (+/-)-mesembranol (1) and (+/-)-O-methyljoubertiamine (2) are described.Each synthesis is developed from a regio- and stereospecific heteroannelation sequence of the respective 1-arylcyclohexanes 4 and 10 to provide the 3a-aryl-cis-octahy
