Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Authors Pasyukov, DV; Chernenko, AY; Shepelenko, KE; Kutyrev, VV; Khrustalev, VN; Chernyshev, VM in ELSEVIER published article about in [Pasyukov, Dmitry, V; Chernenko, Andrey Yu; Shepelenko, Konstantin E.; Kutyrev, Vadim V.; Chernyshev, Victor M.] Platov South Russian State Polytech Univ NPI, Novocherkassk 346428, Russia; [Khrustalev, Victor N.] Peoples Friendship Univ Russia, RUDN Univ, Moscow 117198, Russia; [Khrustalev, Victor N.] Russian Acad Sci, ND Zelinsky Inst Organ Chem, Moscow 119991, Russia in 2021.0, Cited 41.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5
Palladium complexes with N-heterocyclic carbene ligands of a new type containing free NH2 group were obtained by direct palladation of 3-amino-1,4-dialkyl-1,2,4-triazolium salts. These amino-functionalized complexes were found to be a versatile platform for postmodification via reactions of the NH2 group with acyl and sulfonyl chlorides.
Application In Synthesis of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Pasyukov, DV; Chernenko, AY; Shepelenko, KE; Kutyrev, VV; Khrustalev, VN; Chernyshev, VM or concate me.
Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics