1,3-Dipolar cycloaddition reactions can be considered a powerful synthetic tool in the building of heterocyclic rings, with applications in different fields. In this review we focus on the synthesis of biologically active compounds possessing the 1,2,3-triazolecorethrough1,3-dipolarcyclo additionreactions. The 1,2,3-triazole skeleton can be present as a single disubstituted ring, as a linker between two molecules, or embebbed in a polyheterocycle. Thec ycloaddition reactions are usually catalysed by copper or ruthenium. Domino reactions can be achieved through dipolarophile anion formation, generally followed by cyclisation. The variety of attainable heterocyclic structures gives an illustration of the importance of the 1,2,3-triazole core in medicinal chemistry.

1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity, through 1,3-Dipolar Cycloadditions

Francesco Mingoia;
2014

Abstract

1,3-Dipolar cycloaddition reactions can be considered a powerful synthetic tool in the building of heterocyclic rings, with applications in different fields. In this review we focus on the synthesis of biologically active compounds possessing the 1,2,3-triazolecorethrough1,3-dipolarcyclo additionreactions. The 1,2,3-triazole skeleton can be present as a single disubstituted ring, as a linker between two molecules, or embebbed in a polyheterocycle. Thec ycloaddition reactions are usually catalysed by copper or ruthenium. Domino reactions can be achieved through dipolarophile anion formation, generally followed by cyclisation. The variety of attainable heterocyclic structures gives an illustration of the importance of the 1,2,3-triazole core in medicinal chemistry.
2014
Istituto per lo Studio dei Materiali Nanostrutturati - ISMN
Cycloaddition / Nitrogen heterocycles / Domino reactions / Homogeneous catalysis / Enzyme catalysis / Biological activity / Medicinal chemistry
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/301208
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