Author:
Prokhorov A. M.,Kozhevnikov D. N.
Publisher
Springer Science and Business Media LLC
Reference138 articles.
1. E. D. Anderson and D. L. Boger, J. Am. Chem. Soc., 133, 12285 (2011).
2. D. L. Boger, Chem. Rev., 86, 781 (1986).
3. H. Neunhoeffer, in: A. R. Katritzky, C. W. Rees, and E. F. V. Scriven (editors), Comprehensive Heterocyclic Chemistry II, Vol. 6, Pergamon Press, Oxford (1996), p. 507.
4. J. Sauer, in: A. R. Katritzky, C. W. Rees, and E. F. V. Scriven (editors), Comprehensive Heterocyclic Chemistry II, Vol. 6, Pergamon Press, Oxford (1996), p. 901.
5. F. Neese, ORCA – an ab initio, Density Functional and Semiempirical Program Package, Version 2.9.0, Max-Planck-Institutе for Bioinorganiс Chemistry, Mülheim a. d. Ruhr (2012).
Cited by
108 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A New Approach to the Synthesis of [1,2,4]Triazolo[1,5-a]pyrimidines by Reaction of 1,2,4,5-Tetrazines with 2-Aminoxazoles;Журнал общей химии;2024-07-23
2. Synthesis of Novel 6‐(2‐Thienyl)‐2,2′‐Bipyridine Ligands Using “1,2,4‐Triazine” Methodology: an Unexpected Demethylation During the Aza‐Diels‐Alder Reaction with 2,5‐Norbornadiene;ChemistrySelect;2024-07-10
3. 2,5-Di(het)arylpyridines: synthesis by ‘‘1,2,4-triazine’’ methodology and photophysical properties;Chemistry of Heterocyclic Compounds;2024-06
4. Azetidine and cyclopropylamine in the “1,2,4-triazine” methodology for the synthesis of α-functionalized 2,2′-bipyridines;Russian Chemical Bulletin;2024-06
5. Synthesis and Reactions of 3‐Amino‐5,6‐Dimethyl‐l,2,4‐Triazine: DFT Studies, ADME Assay, and Molecular Docking on the new l,2,4‐Triazine Derivatives as Anticancer Agents.;ChemistrySelect;2024-04-22