Amides are versatile building blocks in synthetic organic chemistry, presenting a wide range
of pharmacological applications, and are used as raw materials in industry for the large …

The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann
(1853–1923), is an acid catalyzed rearrangement of an oxime to an amide. The Beckmann …

Amide bond formation reactions are among the most important transformations in organic
chemistry because of the widespread occurrence of amides in pharmaceuticals, natural …

In this report, the synthesis of amides from aldoximes (Beckmann rearrangement) has been
reported using cobalt (II) porphyrin covalently linked to graphene oxide as a nano …

The one-pot conversion of aldehydes to their corresponding primary amides has been
studied using SBA-15-grafted ethylenediamine copper complexes (En–Cu). The …

Well dispersed palladium nanoparticles, with size 3–5 nm, have been immobilized on
APTES functionalized SBA-15 and are found to be efficient and selective catalysts for the …

The rearrangement of aldoximes to primary amides has been studied using the readily
available arene-ruthenium (II) complex [RuCl2 (η6-C6Me6){P (NMe2) 3}](5 mol%) as …

Chemoselective hydrodeoxygenation (HDO) of lignin derivatives is of great importance in
converting biomass into high value-added chemicals. Herein, we report a simple …

Copper (II) acetate is a versatile catalyst for the direct transformation of any type of
aldehydes into primary amides by stoichiometric reaction with hydroxylamine in water. The …

A RhNPs/SBA-NH2 catalyst with< 3 nm sized rhodium nanoparticles has been synthesized
using amine functionalized SBA-15 (SBA-NH2) as support, rhodium acetyl acetonate as a …