Author:
Potts K. T.,Burton H. R.,Bhattacharyya J.
Publisher
American Chemical Society (ACS)
Cited by
82 articles.
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1. Base-Promoted Tandem SNAr/Boulton–Katritzky Rearrangement: Access to [1,2,4]Triazolo[1,5-a]pyridines;Organic Letters;2022-04-20
2. An efficient and metal-free synthetic protocol for mono-, bis-, and spiro[1,2,4]triazolo[1,5-a]pyridines utilizing 1,2-diaminopyridine derivative via C–N bond formation;Synthetic Communications;2021-08-06
3. Toxicity Assessment of Energetic Materials by Using the Luminescent Bacteria Inhibition Test;Propellants, Explosives, Pyrotechnics;2020-10-04
4. A facile, practical and metal-free microwave-assisted protocol for mono- and bis-[1,2,4]triazolo[1,5-a]pyridines synthesis utilizing 1-amino-2-imino-pyridine derivatives as versatile precursors;RSC Advances;2020
5. Trichloroisocyanuric acid-mediated synthesis of 1,5-fused 1,2,4-triazoles from N-heteroaryl benzamidines via intramolecular oxidative N–N bond formation;Tetrahedron Letters;2019-09