Amide bond formation is a fundamentally important reaction in organic synthesis, and is
typically mediated by one of a myriad of so-called coupling reagents. This critical review is …

In this Review, we summarize the current state of the art in late‐transition‐metal‐catalyzed
reactions of acyl fluorides, covering both their synthesis and further transformations. In …

This work describes the application of pentafluoropyridine (PFP), a cheap commercially
available reagent, in the deoxyfluorination of carboxylic acids to acyl fluorides. The acyl …

Abstract N-Methoxy-N-methylamide, popularly addressed as the Weinreb amide, has
surfaced as an amide with a difference. This amide has served as an excellent acylating …

A convenient, highly efficient, and selective transformation of aliphatic and aromatic
carboxylic acids to acyl fluorides is reported. In contrast to established approaches that …

A protocol for amide bond formation with electron deficient amines and sterically hindered
substrates - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB02129D …

Acyl fluorides are versatile acylating agents owing to their unique stability. Their synthesis,
however, can present challenges and is typically accomplished through deoxyfluorination of …

The construction of amide bonds and peptide linkages is one of the most fundamental
transformations in all life processes and organic synthesis. The synthesis of structurally …

3, 3-Difluoro-1, 2-diphenylcyclopropene (CpFluor), a bench-stable fluorination reagent, has
been developed in the deoxyfluorination of carboxylic acids to afford various acyl fluorides …

The first Ni (cod) 2/PPh3 catalyst system has been established for decarbonylative
borylation of aroyl fluorides with bis (pinacolato) diboron. A wide range of functional groups …