Tetrahydroquinoline is one of the most important simple nitrogen heterocycles, being
widespread in nature and present in a broad variety of pharmacologically active …

The present review paper deals with the development of catalytic systems in water in the
presence of micelles obtained by addition of surfactants, focusing on the effects of these …

The quinoline core possesses a vast number of biological activities such as anticancer,
antimalarial, antimicrobial, antifungal, antitubercular and antileishmanial. The conventional …

The Povarov reaction provides a straightforward and modular entry to 1, 2, 3, 4-
tetrahydroquinolines (THQs). Despite its importance, it was only very recently that several …

Quinolines are a prominent heterocyclic motif and crucial building blocks in creating
physiologically active compounds. Due to the fast development of novel medicines with a …

Abstract An oxidative [3+ 2+ 1] cyclization of enaminones and N‐alkenyl‐2‐pyrrolidinone is
described for the synthesis of 4‐alkylated 1, 4‐dihydropyridines (1, 4‐DHPs). By using …

Over the last few decades surface active compounds in aqueous media have proven to be
the most benign alternative for overcoming the difficulty of insolubility and hydrolytic …

Although nature uses the aqueous environment in most of its chemical/biochemical
transformations, water as solvent was totally neglected in organic transformations till the end …

Diels–Alder cycloaddition reaction is one of the most powerful strategies for the construction
of six-membered carbocyclic and heterocyclic systems, in most cases with high regio-and …

An environmentally benign protocol for the synthesis of N-(pyridine-2-yl) amides from
aldehydes and 2-aminopyridines has been developed under mild reaction conditions. This …