The development of metal‐free syntheses toward 1, 2, 3‐triazoles has been a burgeoning
research area throughout the past decade. Despite the numerous advances, the scarceness …

The 1, 3a, 6a-triazapentalene (TAP) is an aromatic heterocyclic fluorescent dye with
interesting features such as its small size, large Stokes shift, solvatochromism, and emission …

Abstract 1, 3a, 6a-Triazapentalene (TAP) is a compact fluorescent chromophore whose
fluorescence properties vary greatly depending on the substituents on the TAP ring. This …

Methyl 4-(1, 3a, 6a-triazapentalen-3-yl) benzoate (TAP1) shows interesting properties as a
small molecule fluorophore. In the search for post-functionalization methods, palladium …

Pyridazino-1, 3a, 6a-triazapentalenes (PyTAP) are compact fused 6/5/5 tricyclic scaffolds
which exhibit promising fluorescent properties. Chemically stable, they can be post …

A multicomponent reaction of triazoloketones, primary amines, and 4-nitrophenyl azide was
developed for the synthesis of hitherto unknown angularly fused/linear bitriazoles. The two …

Analogies between the mechanisms of electrophilic substitution and nucleophilic
substitution have been discussed. Theoretical calculations, involving aromaticity …

The 1, 3a, 6a-triazapentalene (TAP) is an aromatic heterocyclic fluorescent dye with
interesting features such as its small size, large Stokes shift, solvatochromism, and emission …

This chapter reviews pericyclic reactions in general and reactions where a cascade of
concerted processes with transition states representing superpositions of two pericyclic …

N, N‐Dialkyl aniline and aminonaphthalenes undergo oxidative cross‐coupling with
phenols and naphthols using a Cr‐salen catalyst (1) under aerobic conditions. A mechanism …