36200-47-2Relevant articles and documents
Triazoliptycenes: A Twist on Iptycene Chemistry for Regioselective Cross-Coupling to Build Nonstacking Fluorophores
Kang, Taewon,Kim, Hongsik,Lee, Dongwhan
supporting information, p. 6380 - 6383 (2017/12/08)
Triazoliptycene fluorophores have been designed and synthesized, in which a three-dimensional propeller-like iptycene motif is employed to suppress intermolecular π-π stacking in the solid state. Key to the success of this modular synthesis is a stereoelectronic bias imposed by the iptycene scaffold, which assists the desired regioselectivity in the C-N cross-coupling step as the last-stage structure diversification from a common precursor.
Another way to the synthesis of 1,2,3-triazoles
Xu, Beihua,Hu, Yongzhou
, p. 1217 - 1222 (2013/10/21)
The reactions of α-bromoacetophenones with methylhydrazine in refluxing acetic acid generated 2-methyl-4-aryl-2H-[1,2,3]triazoles in good yields. The method was developed by the reactions of α-bromoacetophenones with phenylhydrazines in the presence of cu
Studies on the Hydrazine Derivatives of p-Tolylglyoxal
El Sadek, Mohamed M.
, p. 357 - 359 (2007/10/02)
A number of p-tolylglyoxalmono- and -bishydrazones were synthesized, acylated, and cyclized to the corresponding 1,2,3-triazoles.Some of the reactions of the prepared triazoles were carried out.Analyses and IR and UV spectra of the compounds prepared were recorded.
