The formation of amide bonds is one of the most stimulating emerging areas in organic and
medicinal chemistry. Amides are recognized as central building blocks in a plethora of …

Abstract The Baylis-Hillman (BH) reaction plays a fascinating role in the field of synthetic and
medicinal chemistry. BH adducts and their derivatives have been used as crucial synthons …

Various primary amides have been synthesized using the transamidation of various tertiary
amides under metal-free and mild reaction conditions. When (NH4) 2CO3 reacts with a …

Herein, we describe an intelligent strategy to fabricate nanosheets of graphitic carbon nitride
(gC 3 N 4) decorated with nanorods copper oxide (CuO NRs). Then, the catalytic activity of …

A simple and rapid access to isoquinolone aldehyde scaffolds has been established by a
rhodium-catalyzed reaction between isoquinolone and methoxyallene that forges …

The CN bond of carboxamides is extremely stable under most conditions. The present study
reveals an unconventional approach to the transamidation of primary amides using DCID as …

The functionalization of hydrocarbons represents an attractive approach for the synthesis of
amides. The amide bond is one of the most fascinating functional groups in nature, owing to …

A green, one-pot approach based on the solvothermal amidation of carboxylic acids with
amines has been developed for the synthesis of diverse aliphatic and aromatic amides. It …

A simple Ru (II)‐catalyzed protocol for the alkenylation of isoquinolones with readily
accessible allyl alcohols to generate aldehyde bearing isoquinolones has been developed …

The combination of the catalytic power of amorphous metal‐organic frameworks (aMOFs)
and biocatalysis has greatly boosted the development of novel synthetic strategies due to its …