Textbook in PDF format

Multicomponent synthesis may provide new and green routes for obtaining bioactive heterocycles. These methods produce less organic waste due to no longer removing solvent and other components between reaction steps. It can be applied to the synthesis of heterocycles with reactions such as the Biginelli reaction. This book explores the use of multi-component reactions for various heterocyclic structures with bioactivity.
Discusses multicomponent synthesis as a method for producing bioactive heterocycles.
Explores three-component synthesis of heterocycles, domino reactions, click reactions, magnetic nanocatalyzed reactions and more.
Synthesis of aza-heterocycles via one-pot domino multicomponent reaction approach
One-pot three-component selective annulation strategies for the synthesis of bioactive β-lactam, pyrrole, and pyridine scaffolds
One-pot three-component synthesis of quinolines and some other selective six-membered heterocycles with biological importance
Multicomponent synthesis of biologically prominent tetrahydrobenzoxanthenone derivatives
One-pot five/four-component synthesis of structurally diverse bioactive quinoxaline-annulated spiroheterocycles through the in situ formation of 11H-indeno[1,2-b]quinoxalin-11-ones
Multicomponent synthesis of biologically active quinazolinone derivatives
Recent approaches toward the synthesis of 1,2,3-triazoles using multicomponent techniques
Synthesis of various bioactive tetrazoles via one-pot multicomponent click reactions
L-Proline and its derivatives catalyzed one-pot multicomponent synthesis of biologically promising N- and O-heterocycles
Microwave-assisted solvent-free multicomponent synthesis of bioactive heterocycles
Deep eutectic mixture (DEM)-assisted multicomponent synthesis of heterocycles