Pinacolone (3,3-dimethyl-2-butanone) is an important ketone in organic chemistry. It is a colorless liquid with a slight peppermint or camphor odor. It...

The pinacol–pinacolone rearrangement is a method for converting a 1,2-diol to a carbonyl compound in organic chemistry. The 1,2-rearrangement takes place...

ampicillin and amoxycillin. It was originally prepared by the oxidation of pinacolone with chromic acid and by the hydrolysis of tert-butyl cyanide. Convenient...

coupling reaction from acetone: As a vicinal-diol, it can rearrange to pinacolone by the pinacol rearrangement, e.g. by heating with sulfuric acid: Pinacol...

cis-3-Hexen-1-ol Methyl isobutyl ketone 3-Methyl-2-pentanone Oxepane Pinacolone This set index page lists chemical structure articles associated with...

3-dimethylbutane-2,3-diol and methyl tert-butyl ketone, better known as pinacolone. Pinacolone itself is then used in synthesis for number of pesticides. Additionally...

acid - corresponding carboxylic acid Pivalamide - corresponding amide Pinacolone - corresponding methyl ketone Conant, J. B.; Webb, C. N.; Mendum, W. C...

with Benzophenone and of Methylmagnesium Bromide-Magnesium Bromide with Pinacolone". The Journal of Organic Chemistry. 27 (2): 596. doi:10.1021/jo01049a060...

Thionyl chloride Ethyl diethanolamine Methyl diethanolamine Triethanolamine Pinacolone Dual-use technology Chemical Weapons Convention. Annex on Chemicals. A...

Seebach, Dieter (1988). "Structure and Reactivity of Lithium Enolates. From Pinacolone to SelectiveC-Alkylations of Peptides. Difficulties and Opportunities...