N–Aryl bond formation under copper catalysis has played a pivotal role and has been
extensively used as a key step in the total syntheses of several therapeutic molecules. The …

The in situ formed ruthenium catalytic system ([Ru]/L) was found to be highly selective for the
dehydrogenative coupling reaction of 2-aminophenyl ketones with amines to form …

An efficient Ru doped hydrotalcite catalyzed N-alkylation of benzamides and sulfonamides
with alcohols via borrowing hydrogen catalysis is illustrated. Various primary alcohols …

Quinazolinone is a preferred structural motif with notable pharmacological activity that is
present in a wide range of naturally occurring compounds. A microwave assisted tandem …

A visible-light-driven photoredox-catalyzed nonaqueous oxidative C–N cleavage of N, N-
dibenzylanilines to 2° amides is reported. Further, we have applied this protocol on 2 …

A tandem synthesis of quinazolinones from 2-aminobenzonitriles is demonstrated here by
using an aliphatic alcohol–water system. For this transformation, a cheap and easily …

Here we report a set of direct functionalization methods of unmasked 2-phenylquinazolin-4
(3H)-ones, a privileged alkaloid core, without the installation/removal event of protecting …

A new mixed-linker iron-based MOF VNU-21 [Fe 3 (BTC)(EDB) 2· 12.27 H 2 O] was
synthesized via mixed-linker synthetic strategy using 1, 3, 5-benzenetricarboxylic acid, 4 …

This paper describes a convenient method to synthesize quinazolin-4 (3 H)-ones from
simple and readily available 2-halobenzamides and nitriles. The Lewis acid Cu-catalyzed …

A mild and atom‐economic method was developed for direct and efficient synthesis of
quinazolinones through a transition‐metal‐free aerobic oxidative cascade annulation …