This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. Find sources: "Carboximidate" – news · newspapers · books · scholar · JSTOR(August 2022) (Learn how and when to remove this message)
The carboximidate group
Carboximidates (or more general imidates) are organic compounds, which can be thought of as esters formed between a imidic acid (R-C(=NR')OH) and an alcohol, with the general formula R-C(=NR')OR".
They are also known as imino ethers, since they resemble imines (>C=N-) with an oxygen atom connected to the carbon atom of the C=N double bond.[1]
Carboximidates (or more general imidates) are organic compounds, which can be thought of as esters formed between a imidic acid (R-C(=NR')OH) and an alcohol...
also substrates for many imine reductase enzymes. Enamine Schiff base Carboximidate Oxazolidine Other functional groups with a C=N double bond: oximes,...
fragrances which aim to mimic those odors. List of esters Amide Thioamide Carboximidate Carbamate Xanthate Amidine Cyanate Thiocyanate Selenocyanate Tellurocyanate...
amines as the nucleophile and without the reduction; generated esters, carboximidates or orthoesters. Williams, Jonathan W. (1943). "β-Naphthaldehyde". Organic...
Dimethyl pimelimidate (DMP) is an organic chemical compound with two functional imidate groups. It is usually available as the more stable dihydrochloride...
The Overman rearrangement is a chemical reaction that can be described as a Claisen rearrangement of allylic alcohols to give allylic trichloroacetamides...
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...
Global Information
