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CARBOXIMIDATE

Carboximidate

Carboximidates (or more general imidates) are organic compounds, which can be thought of as esters formed between an imidic acid (R−C(=NR′)OH) and an alcohol

Carboximidate

Imine

Organic compound or functional group containing a C=N bond

also substrates for many imine reductase enzymes. Enamine Schiff base Carboximidate Oxazolidine Other functional groups with a C=N double bond: oximes,

Imine

Ester

Compound derived from an acid

fragrances which aim to mimic those odors. List of esters Amide Thioamide Carboximidate Carbamate IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold

Ester

Chapman rearrangement

The Chapman rearrangement is the thermal conversion of aryl N-arylbenzimidates to the corresponding amides, via intramolecular migration of an aryl group

Chapman rearrangement

Chapman_rearrangement

Dimethyl pimelimidate

Chemical compound

Dimethyl pimelimidate (DMP) is an organic chemical compound with two functional imidate groups. It is usually available as the more stable dihydrochloride

Dimethyl pimelimidate

Dimethyl_pimelimidate

Overman rearrangement

The Overman rearrangement is a chemical reaction that can be described as a Claisen rearrangement of allylic alcohols to give allylic trichloroacetamides

Overman rearrangement

Overman_rearrangement

Mumm rearrangement

The Mumm rearrangement is an organic reaction and a rearrangement reaction. It describes a 1,3(O-N) acyl transfer of an acyl imidate or isoimide group

Mumm rearrangement

Mumm_rearrangement

Stephen aldehyde synthesis

Chemical reaction

amines as the nucleophile and without the reduction; generated esters, carboximidates or orthoesters. Williams, Jonathan W. (1943). "β-Naphthaldehyde". Organic

Stephen aldehyde synthesis

Stephen_aldehyde_synthesis

Lotrifen

Chemical compound

It was described in 1978. Reaction of the acyl hydrazide (1) and the carboximidate (2) gives compound (3). Heating this in the presence of sodium hydride

Lotrifen