ketonic

Reports have shown that the ketonic diet protects against seizures in epilepsy.

Burning of fat causes a ketonic state that may result in an excess of ketones.

In ketonic decarboxylation a carboxylic acid is converted to a ketone.

In ketonic decarboxylation symmetrical ketones are prepared from carboxylic acids.

The ketonic reaction may therefore be either in basic medium or in acidic medium.

This enzyme belongs to the family of hydrolases, specifically those acting on carbon-carbon bonds in ketonic substances.

Mesoxalic acid is both a dicarboxylic acid and a ketonic acid.

A 'thiosemicarbazone' contains a sulfur atom in lieu of the ketonic oxygen in semicarbazone.

Therefore ketonic halogenation accurs.

Previously, acetone was produced by the dry distillation of acetates, for example calcium acetate in ketonic decarboxylation.

This enzyme belongs to the family of transferases, specifically those transferring aldehyde or ketonic groups (transaldolases and transketolases, respectively).

Rotenone is an odourless, colourless, crystalline ketonic chemical compound used as a broad-spectrum insecticide, piscicide, and pesticide.

In 1889, Ernst Beckmann discovered that dissolving menthone in concentrated sulfuric acid gave a new ketonic material.

Like typical hydrated ketonic acids, it is reduced in aqueous solution by sodium amalgam to tartronic acid, and also combines with phenylhydrazine and hydroxylamine.

For example, C-H bonds adjacent to ketonic carbonyl groups can be replaced by C-D bonds, using acid or base catalysis.

Ketones are trigonal planar around the ketonic carbon, with C-C-O and C-C-C bond angles of approximately 120 .

Ketonic decarboxylation (also known as ketonization) is a type of organic reaction and a decarboxylation converting two equivalents of a carboxylic acid to a symmetric ketone by the application of heat with expulsion of one equivalent of water and one equivalent of carbon dioxide.