The copper‐catalyzed alkyne‐azide cycloaddition (CuAAC) is a highly versatile,
regioselective synthesis of 1, 4‐disubstituted 1, 2, 3‐triazoles under mild reaction conditions …

The development of new strategies for synthesis of small-sized heterocycles has remained a
highly attractive but challenging proposition. An overview of the application of microwave …

An efficient and green route for the synthesis of dihydropyrimidinones via microwave-
assisted Biginelli reaction catalyzed by 3 mol% of heteropolyanion-based ionic liquids under …

The objective of this review is to summarize some of the recent advances in a sulfuric acid-
modified polyethylene glycol 6000 (PEG-OSO3H) as a stable, recyclable and bio …

This review focuses on the application of click chemistry in medicinal sciences, and
particularly on its role in drug discovery. Because of its high modularity, click chemistry helps …

A novel iron-catalyzed one-pot multi-component tandem reaction of acetoacetamide, urea,
and two molecules of aryl aldehydes has been developed. This reaction provides a general …

A new and efficient approach for the synthesis of 2, 4, 5-triaryl-1 H-imidazoles linked 1, 4-
disubstitued 1, 2, 3-triazoles have been developed by multicomponent condensation with …

1, 3-dipolar cycloadditions have been studied extensively for decades. The advantages of
this synthetic approach may be increased further by applying microwave irradiation. The …

A number of four-component condensation adducts, which were readily obtained from one-
pot reaction of aryl carboxylic acids, arylaldehydes, arylamines, and c-hexylisocyanide, were …

The Biginelli reaction, a three-component cyclocondensation reaction, is an important
member of the multicomponent reaction (MCR) family. The Biginelli reaction is so efficient …