A series of novel 2,7-naphthyridine derivatives were designed with potential applications in optical switching. The electronic properties and nonlinear optical properties of the designed compounds were extensively studied using DFT.
This review highlights advances in one-pot multicomponent synthesis of naphthyridine derivatives, focusing on efficient, atom-economical methods, diverse scaffolds and mechanistic insights fostering innovation in organic synthesis.
A silver-catalyzed one-pot, regio- and chemoselective synthesis of benzo[b][1,7]- and benzo[c][2,7]-naphthyridines via Michael addition–cyclization is reported, supported by NMR evidence and enabling access to novel perlolidine analogs.
In this investigation, we synthesized pyridonaphthyridines, as a new class of fused heterocyclic compounds, through an efficient multicomponent reaction.
3D current density distribution in TEQ2+ suggests a transformation from antiaromaticity to aromaticity.