✦ LIBER ✦

One-Step Conversion of Azine N-Oxides to α-1,2,4-Triazolo-, 1,2,3-Triazolo, Imidazolo-, and Pyrazoloheteroarenes

✍ Scribed by Keith, John M.

Book ID: 115463115
Publisher: American Chemical Society
Year: 2010
Tongue: English
Weight: 923 KB
Volume: 75
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo1001017

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: One-Step Conversion

ChemInform Abstract: One-Step Conversion of Azine N-Oxides to α-1,2,4-Triazolo-, 1,2,3-Triazolo, Imidazolo-, and Pyrazoloheteroarenes.

✍ John M. Keith 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

One-Step Conversion of Azine N -Oxides t

One-Step Conversion of Azine N -Oxides to α- N -Aryltriflamidoazines

✍ Keith, John M. 📂 Article 📅 2012 🏛 American Chemical Society 🌐 English ⚖ 528 KB

ChemInform Abstract: One Step Conversion

ChemInform Abstract: One Step Conversion of Heteroaromatic-N-Oxides to Imidazolo-Heteroarenes.

✍ John M. Keith 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

The chemistry of polyazaheterocyclic com

The chemistry of polyazaheterocyclic compounds. Part III. The acid-catalysed conversion of [1,2,3]triazolo[5,1-c][1,2,4]benzotriazine derivatives into 1,2,4-benzotriazines and their 1-N-oxides

✍ Tennant, G. 📂 Article 📅 1967 🏛 The Royal Society of Chemistry 🌐 English ⚖ 760 KB

Synthesis of 4H-[1,2,3]triazolo[4,5-c][1

Synthesis of 4H-[1,2,3]triazolo[4,5-c][1,2,5]oxadiazole 5-oxide and its N- and O-alkyl derivatives

✍ Aleksandr M. Churakov; Sema L. Ioffe; Yuri A. Strelenko; Vladimir A. Tartakovsky 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 192 KB

Synthesis of 4H-[1,2,3]triazolo[4,5-c][1

Synthesis of 4H-[1,2,3]triazolo[4,5-c][1,2,5]oxadiazole 5-oxide and its N- and O-alkyl derivatives

✍ Aleksandr M. Churakov; Sema L. Ioffe; Yuri A. Strelenko; Vladimir A. Tartakovsky 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 192 KB

The synthetic route to the fused 1,2,3-triazole 2-oxide systems via intramolecular cyclization of N-nitroso and azido groups is described. The title compounds are characterized by IH, 13C, 14N. 15N and 170 NMR spectroscopy.