EDC (1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide) is a carbodiimide that is well known reagent for the amide coupling reactions between an amine and carboxylic acid in the presence of a base. It is the commonly used coupling agent in industries because it produces a water-soluble urea byproduct, which can be easily removed by an aqueous work-up. However, our methodology, the desired amide product precipitates out of the reaction mixture, and no additional work-up is required.3 Using aqueous micelles of PS-750-M as a solvent dramatically increases the rate of reaction.2 The filtrate recovered can be recycled to perform several coupling runs after post-reaction manipulation
We describe the development of a sustainable ester amidation process. Base and solvent screening, co...
The synthesis of amides is extremely important given the ubiquitous presence of this motif in biolog...
The synthesis of amides is of widespread importance, and there has been considerable recent interest...
Objective: Amide is one of the most important functional group presents in the chemicals, pharmaceut...
A general and environmentally responsible method for the formation of amide/peptide bonds in an aque...
The widespread occurrence of the amide functional group in the pharmaceutical industry and its preva...
A general selective and environmentally friendly method for the formation of amide bonds using a sur...
The construction of the amide/peptide bond is among the most performed transformations in the pharma...
Despite the amide formation reaction being a key reaction in organic chemistry, the direct amide for...
A range of alternative solvents have been evaluated within amidation reactions employing common coup...
A frequent reaction used in organic synthesis is amide bond formation also known as peptide bonds in...
Previously held under moratorium in Chemistry Department (GSK) from 16 April 2018 until 18 June 2021...
Abstract The synthesis of the amide bond between an amine and a carboxylic acid is one of the most s...
Despite being one of the most frequently carried out chemical reactions in industry, there is curren...
The biocatalytic synthesis of amides from carboxylic acids and primary amines in aqueous media can b...
We describe the development of a sustainable ester amidation process. Base and solvent screening, co...
The synthesis of amides is extremely important given the ubiquitous presence of this motif in biolog...
The synthesis of amides is of widespread importance, and there has been considerable recent interest...
Objective: Amide is one of the most important functional group presents in the chemicals, pharmaceut...
A general and environmentally responsible method for the formation of amide/peptide bonds in an aque...
The widespread occurrence of the amide functional group in the pharmaceutical industry and its preva...
A general selective and environmentally friendly method for the formation of amide bonds using a sur...
The construction of the amide/peptide bond is among the most performed transformations in the pharma...
Despite the amide formation reaction being a key reaction in organic chemistry, the direct amide for...
A range of alternative solvents have been evaluated within amidation reactions employing common coup...
A frequent reaction used in organic synthesis is amide bond formation also known as peptide bonds in...
Previously held under moratorium in Chemistry Department (GSK) from 16 April 2018 until 18 June 2021...
Abstract The synthesis of the amide bond between an amine and a carboxylic acid is one of the most s...
Despite being one of the most frequently carried out chemical reactions in industry, there is curren...
The biocatalytic synthesis of amides from carboxylic acids and primary amines in aqueous media can b...
We describe the development of a sustainable ester amidation process. Base and solvent screening, co...
The synthesis of amides is extremely important given the ubiquitous presence of this motif in biolog...
The synthesis of amides is of widespread importance, and there has been considerable recent interest...