106736-30-5Relevant academic research and scientific papers
Designing a new basic ionic liquid [DHIM][OH] as a task specific bifunctional catalyst for facile microwave assisted metal free synthesis of 5-amino-1,2,3-triazoles
Dutta, Bidyutjyoti,Garg, Anirban,Kulshrestha, Akshay,Kumar, Arvind,Phukan, Parmita,Sarma, Diganta
supporting information, p. 12792 - 12797 (2021/08/04)
A green protocol for the synthesis of a series of 5-amino-1,2,3-triazoles from benzyl cyanide and phenyl azide derivatives catalyzed by the novel bifunctional ionic liquid [DHIM][OH] under microwave irradiation has been developed. The bifunctional ionic l
One-Pot Synthesis of 5-Amino-1,2,3-triazole Derivatives via Dipolar Azide?Nitrile Cycloaddition and Dimroth Rearrangement under Solvent-Free Conditions
Gribanov, Pavel S.,Atoian, Edita M.,Philippova, Anna N.,Topchiy, Maxim A.,Asachenko, Andrey F.,Osipov, Sergey N.
supporting information, p. 1378 - 1384 (2021/02/26)
An efficient one-pot methodology for the preparation of 5-amino-1,2,3-triazole derivatives based on the combination of dipolar azide?nitrile cycloaddition with Dimroth rearrangement under solvent-free conditions has been developed.
INFLUENCE OF ELECTRON-WITHDRAWING N-1 SUBSTITUENTS ON THE THERMAL BEHAVIOUR OF S-AZIDO-1,2,3-TRIAZOLES
L'Abbe, Gerrit,Beenaerts, Linda
, p. 749 - 756 (2007/10/02)
5-Amino-1,2,3-triazoles (7), possessing a strong electron-withdrawing N-1 substituent, cannot be converted into the corresponding azides by the diazotization method, but the diazo transfer on the conjugate bases with tosyl azide proceeds smoothly and was
