Litcius/Paper detail

Fast Amide Couplings in Water: Extraction, Column Chromatography, and Crystallization Not Required

Sudripet Sharma, Nicklas W. Buchbinder, Wilfried M. Braje, Sachin Handa

2020Organic Letters85 citationsDOI

Abstract

In the micelle of PS-750-M, the presence of 3° amides from the surfactant proline linker mimics dimethylformamide, dimethylacetamide, and N-methyl-2-pyrrolidone. The resultant micellar properties enable extremely fast amide couplings mediated by 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (without hydroxybenzotriazole), rather than expensive and specialized coupling agents. Conditions have been developed wherein products precipitate, and isolation by filtration completely avoids the use of organic solvent. This methodology is scalable and avoids product epimerization.

Topics & Concepts

ChemistryLinkerAmideCarbodiimideDimethylformamidePulmonary surfactantDimethylacetamideExtraction (chemistry)SolventCrystallizationMicelleChromatographyOrganic chemistryCombinatorial chemistryAqueous solutionOperating systemComputer scienceBiochemistryChemical Synthesis and AnalysisAnalytical Chemistry and ChromatographyCarbohydrate Chemistry and Synthesis
Fast Amide Couplings in Water: Extraction, Column Chromatography, and Crystallization Not Required | Litcius