67519-00-0

Upstream product

• 15780-34-4 1-(3,3-Dimethyl-bicyclo<2.2.1>hept-2-yl)ethanon 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 542-92-7 cyclopenta-1,3-diene 
• 472-17-3 exo-3,3-dimethyl-2-norbornanacetaldehyde 
• 124024-32-4 2-endo-10,10-diacetoxycamphane 
• 875-03-6 Camphene epoxide 
• 565-00-4 dl-camphene 
• 52363-25-4 camphenilone 
• 15780-45-7 (+/-)-1-(3,3-dimethyl-norborn-5-ene-2-endo-yl)-ethanone 

Downstream Products

• 18310-55-9 (3,3-dimethylbicyclo[2.2.1]heptan-2-yl)methanol 
• 472-17-3 exo-3,3-dimethyl-2-norbornanacetaldehyde 
• 61175-88-0 (+/-)-isocamphenilanic acid-chloride 
• 85099-15-6 3-((1S,2R,4R)-3,3-Dimethyl-bicyclo[2.2.1]hept-2-yl)-propionyl chloride 

Relevant academic research and scientific papers

Oxygenation of Oleefinic Hydrocarbons Catalyzed by Iron(II) Acetonitrile Solvate

Oxygenation reactions of olefins having an endo- or exo-cyclic double bond, namely, cyclohexene, norbornene, camphene, longifolene, and ent-kaurene, with a simple model reagent, Fe(MeCN)62+-H2O2-Ac2O, for mono-oxygenase were investigated in connection with their biotransformations.Keywords oxygenation; olefin; endo-cyclic double bond; exo-cyclic double bond; iron(II) acetonitrile solvate; hydrogen peroxide; model enzyme; mono-oxygenase

Chromic Acid Oxidation of Some Oxiranes

Oxiranes derived from some alkenes, with olefinic bonds present in different stereoelectronic environments, have been treated with Cr(VI)-reagents.The major products obtained have been identified and their formation rationalized.In some cases, the method becomes synthetically useful for C-C bond cleavage.