Hirsjarvi, Pekka published the artcileFormation of camphene glycol carbonate in the oxidation of camphene with SeO2, Application of 2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol, the main research area is .
cf. CA 53, 16194g. Camphene glycol carbonate (I), m. 147-8° was separated by distillation or adsorption chromatog. from the oxidation products of camphene with SeO2 in boiling Ac2O. Alk. hydrolysis of I yielded camphene glycol (II), m. 196-8°. II formed a mono-p-tosylate, m. 84.5-7.0°, which formed camphene hydrate, m. 152-5° on reduction with LiAlH4. The formation of I by SeO2 is a stereospecific reaction.
Suomen Kemistilehti B published new progress about Oxidation. 42822-86-6 belongs to class alcohols-buliding-blocks, name is 2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol, and the molecular formula is C10H20O2, Application of 2-(2-Hydroxypropan-2-yl)-5-methylcyclohexanol.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts