Huisgen Cycloaddition of Azidoazulenes: Synthesis, Structural and Optical Properties of 2- and 6-(1,2,3-Triazol-1-yl)azulenes.

ABSTRACT: We developed an efficient and modular route to 2- and 6-(1,2,3-triazol-1-yl)azulenes to expand the synthetic accessibility and functional scope of azulene-based π-systems with stimulus-responsive photophysics. Readily accessible 2- and 6-azidoazulenes, prepared in excellent yields via S_NAr reactions of haloazulenes, were subjected to Cu(I)-catalyzed Huisgen [3 + 2] cycloaddition with a broad range of terminal alkynes to afford the corresponding triazolylazulenes in good to high yields, followed by acid-mediated decarboxylation and Staudinger reduction to enable further diversification to 2-azulenyltriazoles and a 6-aminoazulene derivative. Single-crystal X-ray diffraction analysis revealed substitution-position-dependent torsional arrangements and variations in π-conjugation bet

SUBMITTER: Shoji T 

PROVIDER: S-EPMC12843792 | biostudies-literature | 2026 Jan

REPOSITORIES: biostudies-literature