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 …

The present review article focuses on the recent advancements in amide and peptide
coupling reactions of racemization-prone substrates using n-propylphosphonic anhydride …

Efficient Copper(II)‐Catalyzed Transamidation of Non‐Activated Primary Carboxamides and
Ureas with Amines × Close The Infona portal uses cookies, ie strings of text saved by a …

Catalytic activation of hydroxyl functionalities is of great interest for the production of
pharmaceuticals and commodity chemicals. Here, 2-alkoxycarbonyl-and 2-phenoxycarbonyl …

Propylphosphonic anhydride (® T3P) promotes cyclization of o-aminobenzenethiol, o-
aminophenol, and o-phenylenediamine with carboxylic acids under microwave irradiation …

Discovered over a century ago, Beckmann rearrangement is still today fully compliant with
all the green chemistry principles and consistent with the key aspects of sustainable …

Direct transamidation of secondary amides was developed via nickel catalysis. In the
presence of trimethylsilyl chloride and manganese, Ni (diglyme) Cl2 with a Briphos ligand …

A new strategy for thiazoles via copper-catalyzed [3+ 1+ 1]-type condensation reaction from
oximes, anhydrides and potassiumthiocyanate (KSCN) is developed herein. The …

An efficient one-pot synthesis of coumarins mediated by propylphosphonic anhydride (T3P) via
the Perkin condensation - ScienceDirect Skip to main contentSkip to article Elsevier logo …

The ecofriendly ternary blend polymer film was prepared from the chitosan (CH), polylactic
acid (PLA) and polyvinyl alcohol (PVA). Immobilization of Candida cylindracea lipase (CCL) …