Explore: Schmidt Reaction

In organic chemistry, the Schmidt reaction is an organic reaction in which an azide reacts with a carbonyl derivative, usually an aldehyde, ketone, or

An aldol condensation is a condensation reaction in organic chemistry in which two carbonyl moieties (of aldehydes or ketones) react to form a β-hydroxyaldehyde

In organic chemistry, the Claisen–Schmidt condensation is the reaction between an aldehyde or ketone having an α-hydrogen with an aromatic carbonyl compound

rearrangement. Lactams form from cyclic ketones and hydrazoic acid in the Schmidt reaction. Cyclohexanone with hydrazoic acid, forms ε - Caprolactum, which upon

synthesis Bohn–Schmidt reaction Boord olefin synthesis Borodin reaction Borsche–Drechsel cyclization Bosch–Meiser urea process Bosch reaction Bouveault aldehyde

name, Mys Shmidta Schmidt reaction Schmidt number Schmidt decomposition, a decomposition of vectors of tensor product spaces Schmidt sting pain index,

Mumm rearrangement Photochemical rearrangement Pinacol rearrangement Schmidt reaction Thermal rearrangement of aromatic hydrocarbons Tiemann rearrangement

The Bohn–Schmidt reaction, a named reaction in chemistry, introduces a hydroxy group at an anthraquinone system. The anthraquinone must already have at

{\displaystyle {\ce {ROH + NH3 -> RNH2 + H2O}}} Unlike the reaction of amines with alcohols the reaction of amines and ammonia with alkyl halides is used for

of the Hammett equation in the prediction of product ratios in the Schmidt reaction of unsymmetrical diarylethylenes: II. The synthesis of possible emetine