In organic chemistry, the Malaprade reaction or Malaprade oxidation is a glycol cleavage reaction in which a vicinal diol is oxidized by periodic acid...

The Lemieux–Johnson or Malaprade–Lemieux–Johnson oxidation is a chemical reaction in which an olefin undergoes oxidative cleavage to form two aldehyde...

acid will cleave vicinal diols into two aldehyde or ketone fragments (Malaprade reaction). This can be useful in determining the structure of carbohydrates...

aldehydes using lead tetraacetate. It is analogous to the use of periodate (Malaprade reaction) but uses a milder oxidant. This oxidation was discovered by...

Tellier – vocals (track 5) Adrian Edeline – guitar (track 12) Gabriel Malaprade – guitar (track 8) Nicolas Bogue – guitar (track 7) Adrien Soleiman –...

of this is diol cleavage, which was also the first to be discovered (Malaprade reaction). In addition to diols, periodates can cleave 1,2-hydroxy ketones...

rearrangement Lucas' reagent Luche reduction Maillard reaction Madelung synthesis Malaprade reaction, Periodic acid oxidation Malonic ester synthesis Mannich reaction...

Banquet, and The movement towards knowledge) were designed by Françoise Malaprade. Albert Ronsin directed the Museum and the Library from 1960 to 1990,...

tetraacetate (Pb(OAc)4). These I- and Pb-based methods are called the Malaprade reaction and Criegee oxidation, respectively. The former is favored for...

iodine(VII) are presumed intermediates in the periodate cleavage of diols (Malaprade reaction), although no carbon-iodine(VII) bond is present in this process...