25108-33-2Relevant academic research and scientific papers
Comparison of 1-Ethyl-5H-tetrazole and 1-Azidoethyl-5H-tetrazole as Ligands in Energetic Transition Metal Complexes
Wurzenberger, Maximilian H. H.,Gruhne, Michael S.,Lommel, Marcus,Szimhardt, Norbert,Klap?tke, Thomas M.,Stierstorfer, J?rg
, p. 2018 - 2028 (2019)
Energetic coordination compounds (ECC) based on 3d or 4d transition metals show promising characteristics to be used as potential replacements for highly toxic lead-containing primary explosives. Herein we report the synthesis of 12 new ECC based on 1-azi
Polymer-Supported Fe-Phthalocyanine Derived Heterogeneous Photo-Catalyst for the Synthesis of Tetrazoles Under Visible Light Irradiation
Khajone, Vijay Baburao,Balinge, Kamlesh Rudreshwar,Bhagat, Pundlik Rambhau
, p. 1948 - 1960 (2020/11/23)
Abstract: Herein, a polymer supported Fe-Phthalocyanine entangled with carboxyl functionalized benzimidazolium moiety (PSFePcCFBM) explored as heterogenous photocatalyst, for regioselective synthesis of 1H-tetrazoles from sodium azide and other affordable
Microwave alkylation of lithium tetrazolate
Müller, Danny,Knoll, Christian,Weinberger, Peter
, p. 131 - 137 (2017/01/17)
Abstract: N1-substituted tetrazoles are interesting ligands in transition metal coordination chemistry, especially in the field of spin crossover. Their synthesis is performed in most cases according to the Franke-synthesis, using a primary amine as reagent introducing the substitution pattern. To enhance flexibility in means of substrate scope, we developed a new protocol based on alkylation of lithium tetrazolate with alkyl bromides. The N1–N2 isomerism of the tetrazole during the alkylation was successfully suppressed by use of highly pure lithium tetrazolate and 30?vol.% aqueous ethanol as solvent, leading to pure N1-substituted products. The feasibility of this reaction was demonstrated by a selection of different substrates. Graphical abstract: [Figure not available: see fulltext.]
REACTIONS OF TRIMETHYLSILYL AZIDE WITH ALDEHYDES: FACILE AND CONVENIENT SYNTHESES OF DIAZIDES, TETRAZOLES, AND NITRILES
Nishiyama, Kozaburo,Oba, Makoto,Watanabe, Akio
, p. 693 - 700 (2007/10/02)
The reactions of trimethylsilyl azide (TMSA) with various aldehydes were found to be versatile procedures for the synthesis of gem- and 1,3-diazides, tetrazoles, and nitriles, whose formation was varied by controlling the quantities of TMSA, catalyst, and the reaction conditions.
SYNTHESIS OF 1-SUBSTITUTED TETRAZOLES BY HETEROCYCLIZATION OF PRIMARY AMINES, ORTHOFORMIC ESTER, AND SODIUM AZIDE
Gaponik, P. N.,Karavai, V. P.,Grigor'ev, Yu. V.
, p. 1255 - 1258 (2007/10/02)
It has been shown that the reaction of heterocyclization of primary amines with orthoformic acid and sodium azide in acetic acid has a rather general character and is a convenient method for the synthesis of 1-substituted tetrazoles.On the basis of experimental data, a probable reaction mechanism is proposed.
