361481-38-1Relevant articles and documents
A fascinating click strategy to novel 1,2,3-triazolium based organic-inorganic hybrids for highly accelerated preparation of tetrazolopyrimidines
Keshavarz, Mosadegh,Taib, Layla A.
, (2022/01/03)
Herein, click reaction is used for the preparation of novel organic-inorganic Br?nsted acidic ionic solids (BAISs) as new catalysts for the efficient synthesis of tetrazolopyrimidines. A series of mono and disubstituted-1,2,3-triazoles were synthesized un
Ammonium Chloride as an Effective Catalyst for the Synthesis of Biologically Active Dihydrotetrazolo[1, 5-a]pyrimidine Carboxylates
Bhagare, Arun M.,Gaware, Manoj R.,Lokhande, Dnyaneshwar. D.
, p. 621 - 624 (2021/01/25)
Various substituted dihydrotetrazolo[1,5-a] pyrimidine carboxylates have been synthesized by reacting aromatic aldehydes, ethyl acetoacetate, and 5-aminotetrazole in one-pot using catalytic amount of ammonium chloride (NH4Cl) under solvent-free
Iodine catalyzed one-pot multicomponent synthesis of a library of compounds containing tetrazolo[1,5-a]pyrimidine core
Zeng, Li-Yan,Cai, Chun
scheme or table, p. 35 - 40 (2010/10/03)
Versatile and novel reactions of 5-aminotetrazole with structurally diverse aryl aldehydes and building blocks with active methylene catalyzed by iodine were investigated in a multicomponent one-pot protocol. A series of 5,7-diaryl-4,7-dihydrotetrazolo[1,
