90645-54-8Relevant academic research and scientific papers
Ductile Pd-Catalysed Hydrodearomatization of Phenol-Containing Bio-Oils Into Either Ketones or Alcohols using PMHS and H2O as Hydrogen Source
Di Francesco, Davide,Subbotina, Elena,Rautiainen, Sari,Samec, Joseph S. M.
supporting information, p. 3924 - 3929 (2018/09/14)
A series of phenolic bio-oil components were selectively hydrodearomatized by palladium on carbon into the corresponding ketones or alcohols in excellent yields using polymethylhydrosiloxane and water as reducing agent. The selectivity of the reaction was governed by the water concentration where selectivity to alcohol was favoured at higher water concentrations. As phenolic bio-oil examples cardanol and beech wood tar creosote were studied as substrate to the developed reaction conditions. Cardanol was hydrodearomatized into 3-pentadecylcyclohexanone in excellent yield. From beech wood tar creosote, a mixture of cyclohexanols was produced. No hydrodeoxygenation occurred, suggesting the applicability of the reported method for the production of ketone-alcohol oil from biomass. (Figure presented.).
A multifunction Pd/Sc(OTf)3/ionic liquid catalyst system for the tandem one-pot conversion of phenol to ε-caprolactam
Shin, Ju Yeon,Jung, Da Jung,Lee, Sang-Gi
supporting information, p. 525 - 528 (2013/05/09)
A multifunction Pd/Sc(OTf)3/ionic liquid catalyst for the tandem one-pot conversion of phenol to ε-caprolactam is reported. Pd and Sc(OTf)3 cooperate to catalyze the hydrogenation of phenol to cyclohexanone with excellent conversion (>99.9%) and selectivity (>99.9%), whereas Sc(OTf)3 and an ionic liquid, [bmim][PF6], cooperate to catalyze the tandem transformation of the resulting cyclohexanone to cyclohexanone oxime and the Beckmann rearrangement affording ε-caprolactam.
Novel cuticular hydrocarbons from the cane beetle Antitrogus parvulus - 4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes. Unprecedented anti-anti-anti-stereochemistry in the 4,6,8,10-methyltetrad
Chow, Sharon,Fletcher, Mary T.,Lambert, Lynette K.,Gallagher, Oliver P.,Moore, Christopher J.,Cribb, Bronwen W.,Allsopp, Peter G.,Kitching, William
, p. 1808 - 1827 (2007/10/03)
(Chemical Equation Presented) The major cuticular hydrocarbons from the cane beetle species Antitrogus parvulus are 4,6,8,10,-16-penta- and 4,6,8,10,16,18-hexamethyldocosanes, 1 and 2, respectively. Stereoisomers of 2,4,6,8-tetramethylundecanal of establi
