Triazoles are important five-membered heterocyclic scaffold due to their extensive biological
activities. This framework can be readily obtained in good to excellent yields on the …

Triazoles find applications in several major technological areas, and especially in drug
discovery. The click-chemistry approaches based on Huisgen's cycloaddition reaction are …

The present feature article describes the different organocatalytic routes for the synthesis of
substituted 1, 2, 3-triazoles. This methodology has recently gained much attention due to its …

Metal-free 1, 3-dipolar cycloaddition reactions have proven to be a powerful tool for the
assembly of key heterocycles, in particular diversely functionalized 1, 2, 3-triazoles. A …

Organocatalytic click! Recent advances in the metal‐free enamine/enolate‐mediated azide–
carbonyl [3+ 2] cycloaddition reaction are discussed. These approaches require neither a …

The construction of 1, 5-disubstituted 1, 2, 3-triazoles has been effected through the cascade
dual C–N bond formation, N–N bond formation and an acyl migration-based C–C bond …

An enolate‐mediated organocatalytic azide–ketone [3+ 2]‐cycloaddition (OrgAKC) reaction
of a variety of enolizable arylacetones and deoxybenzoins with aryl azides was developed …

Click chemistry is one of the most efficient and widely used methodologies for selective C–N
bond forming reactions, encompassing the synthesis of 1, 2, 3-triazoles, and it has been …

In this review, authors focus mostly on the various synthetic strategies developed so far for 1,
2, 3-triazole scaffold and its derivatives via different approaches such as metal-free, metal …

A combined tris (trimethylsilyl) silane and visible-light-promoted intramolecular reductive
cyclization protocol for the synthesis of indoles and oxindoles has been developed. This …