Category: 77451-51-5

Kluge, R.; Schulz, M.; Liebsch, S. published an article on February 19 ,1996. The article was titled 《Diastereoselective Epoxidation of Olefins by Organo Sulfonic Peracids. II》, and you may find the article in Tetrahedron.Name: 3-Nitro-1-tosyl-1H-1,2,4-triazole The information in the text is summarized as follows:

The behavior of sulfonic peracids (generated in situ) toward olefins, allylic alcs., homoallylic alcs., and α,β-unsaturated ketones was studied. For example, 4-methylbenzenesulfonoperoxoic acid was generated in situ from 1-(4-methylphenylsulfonyl)-1H-imidazole and trimethyloxonium tetrafluoroborate. Epoxidation of α-pinene with 4-methylbenzenesulfonoperoxoic acid gave 2α,3α-epoxypinane. Generally, the epoxidation proceeds in a peracid-like manner with greater diastereoselectivity than those by common oxidants. In particular, the epoxidation of Δ4 3-ketosteroids gave 4α,5α-epoxides with good diastereoselectivity. Enhanced α-selectivity was also found in the epoxidation of a cholesterol derivative The results came from multiple reactions, including the reaction of 3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5Name: 3-Nitro-1-tosyl-1H-1,2,4-triazole)

3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties Name: 3-Nitro-1-tosyl-1H-1,2,4-triazole

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Recommanded Product: 3-Nitro-1-tosyl-1H-1,2,4-triazoleOn November 15, 1980 ,《Synthesis of the 3′-terminal decaribonucleoside nonaphosphate of yeast alanine transfer ribonucleic acid》 appeared in Tetrahedron. The author of the article were Jones, S. S.; Rayner, B.; Reese, C. B.; Ubasawa, A.; Ubasawa, M.. The article conveys some information:

The yeast decaribonucleotide UpCpGpUpCpCpApCpCpA was prepared from the 5 nucleosides I (R = 4-N-benzoylcytosin-1-yl, 2-N-benzoylguanin-9-yl), II (R = 6-N-benzoyladenin-9-yl, uracil-1-yl), and III (R = 6-N-benzoyladenin-9-yl) by the phosphotriester method. The use of o-dibromomethylbenzoyl as a protecting group in oligoribonucleotide synthesis is described. The internucleotide linkages were protected by o-chlorophenyl groups, which were readily removed by the N1,N1,N3,N3-tetramethylguanidinium salt of syn-4-nitrobenzaldoxime. The 1st phosphorylation step was carried out by treatment with o-chlorophenylphosphorodi(1,2,4-triazolide) followed by H2O and Et3N. The triazole IV was used as the activating agent in the 2nd phosphorylation step. In the part of experimental materials, we found many familiar compounds, such as 3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5Recommanded Product: 3-Nitro-1-tosyl-1H-1,2,4-triazole)

3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties Recommanded Product: 3-Nitro-1-tosyl-1H-1,2,4-triazole

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Holzer, Wolfgang published an article in Tetrahedron. The title of the article was 《Spectral and structural assignments with various N-substituted 1,2,4-triazoles: NOE difference spectroscopy as a powerful tool》.Computed Properties of C9H8N4O4S The author mentioned the following in the article:

The unambiguous discrimination between signals due to H-3 and H-5 in various 1-substituted 1H-1,2,4-triazoles as well as the differentiation between isomeric 1,3-, 1,5- and 3,4-disubstituted 1,2,4-triazoles by means of NOE difference spectroscopy is described. The assignments based on NOE difference experiments are shown to agree with those resting on triazole 13C,1H spin-coupling constants The experimental part of the paper was very detailed, including the reaction process of 3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5Computed Properties of C9H8N4O4S)

3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties Computed Properties of C9H8N4O4S

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

《High-yield synthesis of oligoribonucleotides using o-nitrobenzyl protection of 2′-hydroxyls》 was written by Hayes, J. A.; Brunden, M. J.; Gilham, P. T.; Gough, G. R.. Application In Synthesis of 3-Nitro-1-tosyl-1H-1,2,4-triazole And the article was included in Tetrahedron Letters in 1985. The article conveys some information:

Use of published procedures for photolytic removal of 2′-O-(o-nitrobenzyl) substituents from model oligoribonucleotides results in low yields of fully-deprotected products accompanied by significant amounts of oligomers carrying altered, UV light-resistant residues derived from the 2′-blocking groups. The efficiency of the deprotection has depends on pH; the side-reactions are avoided when the photolysis is carried out in solution buffered at pH 3.5. In the experiment, the researchers used many compounds, for example, 3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5Application In Synthesis of 3-Nitro-1-tosyl-1H-1,2,4-triazole)

3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties Application In Synthesis of 3-Nitro-1-tosyl-1H-1,2,4-triazole

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

《One-Step Conversion of Azine N-Oxides to α-1,2,4-Triazolo-, 1,2,3-Triazolo, Imidazolo-, and Pyrazoloheteroarenes》 was written by Keith, John M.. SDS of cas: 77451-51-5 And the article was included in Journal of Organic Chemistry on April 16 ,2010. The article conveys some information:

Pyridine, quinoline, isoquinoline, azaindole, and pyrimidine N-oxides, e.g. I, were converted to their α-triazole and α-diazole derivatives, e.g. II, by treatment with the corresponding p-toluenesulfonylazoles and Hunig’s base at elevated temperatures In the experimental materials used by the author, we found 3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5SDS of cas: 77451-51-5)

3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties SDS of cas: 77451-51-5

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Peyman, Anusch; Uhlmann, Eugen; Wagner, Konrad; Augustin, Sascha; Breipohl, Gerhard; Will, David W.; Schaefer, Andrea; Wallmeier, Holger published their research in Angewandte Chemie, International Edition in English on December 6 ,1996. The article was titled 《Phosphonic ester nucleic acids (PHONAs): oligodeoxyribonucleotide analog with an achiral phosphonic acid ester backbone》.COA of Formula: C9H8N4O4S The article contains the following contents:

The preparation of polyamide nucleic acid analogs with an achiral and neg. charged backbone to which the nucleobases are attached through carboxymethylene linkers, is reported. The experimental part of the paper was very detailed, including the reaction process of 3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5COA of Formula: C9H8N4O4S)

3-Nitro-1-tosyl-1H-1,2,4-triazole(cas: 77451-51-5) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties COA of Formula: C9H8N4O4S

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics