“…The Mg(0) metal has been applied in various reduction and coupling reactions, where most of the reactions were reported using a large amount of magnesium metal. Comparatively, fewer catalytic transformations have been found in the literature using commercially available Mg metal as a catalyst, although it is less expensive than other Mg-based catalytic systems. However, various catalytic reactions, including hydroboration of carbonate, nitrile, and esters, and enantioselective catalytic transformations have been developed using Mg complexes .…”
“…The Mg(0) metal has been applied in various reduction and coupling reactions, where most of the reactions were reported using a large amount of magnesium metal. Comparatively, fewer catalytic transformations have been found in the literature using commercially available Mg metal as a catalyst, although it is less expensive than other Mg-based catalytic systems. However, various catalytic reactions, including hydroboration of carbonate, nitrile, and esters, and enantioselective catalytic transformations have been developed using Mg complexes .…”
Furan heterocyclic compounds derived from renewable sources are popular versatile candidates for the production of multifunctional macromolecular materials. These compounds are also used as hydrophobilization monomers for reversible polyadducts or as versatile building blocks in Diels‐Alder reactions. In the present study, an efficient approach to chemoselective acylation of furfurylamine with a series of non‐preactivated monocarboxylic or dicarboxylic long‐chain fatty acids and some of their functionalized derivatives has been achieved via catalytic direct amidation in reversed micellar medium. A convenient and environmentally friendly method has been developed for furfurylamides via a dehydrative coupling reaction. For this purpose, a new cationic Brønsted‐type sulfonic acid catalyst containing a hexadecyl alkyl chain was synthesized and fully characterized. The present catalytic reaction produced the respective N‐furfurylamides materials in good to excellent yields. This study also confirms that the direct amidation of carboxylic acids with selected amine compounds can be successfully catalyzed by Brønsted acids. Its simplicity and high atom economy are the main advantages of this method.
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