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An Example of Polynomial Expansion: The Reaction of 3(5)-Methyl-1H-Pyrazole with Chloroform and Characterization of the Four Isomers
Vera L. M. Silva, Artur M. S. Silva, Rosa M. Claramunt, Dionisia Sanz, Lourdes Infantes, Ángela Martínez-López, Felipe Reviriego, Ibon Alkorta and José Elguero Molecules 24(3) 568 (2019) https://doi.org/10.3390/molecules24030568
New bipyrazolic compounds: Synthesis, characterization, antibacterial activity and computational studies
The Structure of N‐phenyl‐pyrazoles and Indazoles: Mononitro, Dinitro, and Trinitro Derivatives
Rosa M. Claramunt, Dolores Santa María, Ibon Alkorta and José Elguero Journal of Heterocyclic Chemistry 55(1) 44 (2018) https://doi.org/10.1002/jhet.3026
New generation of tetrapyrazolic macrocycles: Synthesis and examination of their complexation properties and antibacterial activity
The 1H NMR spectrum of pyrazole in a nematic phase
Patricio Provasi, María Luisa Jimeno, Ibon Alkorta, Felipe Reviriego, José Elguero and Jukka Jokisaari Magnetic Resonance in Chemistry 54(8) 637 (2016) https://doi.org/10.1002/mrc.4422
Copper‐Catalyzed Arylation of Nitrogen Heterocycles from Anilines under Ligand‐Free Conditions
Dounia Toummini, Anis Tlili, Julien Bergès, Fouad Ouazzani and Marc Taillefer Chemistry – A European Journal 20(45) 14619 (2014) https://doi.org/10.1002/chem.201404982
The NMR study of long-range spin–spin coupling: Peculiarities of molecular structure of N-vinylpyrazole derivatives
The tautomeric structures of 3(5),3′(5′)-azopyrazole [(E)-1,2-di(1H-pyrazol-3(5)-yl)diazene)]: The combined use of NMR and electronic spectroscopies with DFT calculations
Mild Copper‐Catalyzed Vinylation Reactions of Azoles and Phenols with Vinyl Bromides
Marc Taillefer, Armelle Ouali, Brice Renard and Jean‐Francis Spindler Chemistry – A European Journal 12(20) 5301 (2006) https://doi.org/10.1002/chem.200501411
Mild Conditions for Copper‐Catalysed N‐Arylation of Pyrazoles
Henri‐Jean Cristau, Pascal P. Cellier, Jean‐Francis Spindler and Marc Taillefer European Journal of Organic Chemistry 2004(4) 695 (2004) https://doi.org/10.1002/ejoc.200300709
Preparation of 1H‐pyrazole‐5‐carboxamides from dilithiated C(α), N‐phenylhydrazones and lithiated ethyl oxanilates or lithiated ethyl oxamate
Jennifer R. Downs, Stefan J. Pastine, Deborah A. Schady, Heather A. Greer, Wayne Kelley, Mildred C. Embree, Jessica D. Townsend and Charles F. Beam Journal of Heterocyclic Chemistry 38(3) 691 (2001) https://doi.org/10.1002/jhet.5570380325
The structure of the compounds resulting from the reaction of arylhydrazines with dehydroacetic acid: an NMR and crystallographic study
Structure of bis-, tris- and tetrakispyrazolylborates in the solid state (sodium and potassium salts of tetrakispyrazolylborate by X-ray crystallography) and in solution (1H, 11B, 13C and 15N NMR)
El Mostafa Tjiou, Alain Fruchier, Valdo Pllegrin and Georges Tarrago Journal of Heterocyclic Chemistry 26(4) 893 (1989) https://doi.org/10.1002/jhet.5570260402
Apurinic DNA reactivity: Modelisation of apurinic DNA breakage with phenylhydrazine and formation of a pyrazole adduct
1H, 13C and 15N NMR spectra of [1,2‐15N2]pyrazole derivatives
Alain Fruchier, Valdo Pellegrin, Rosa Maria Claramunt and Jose Elguero Organic Magnetic Resonance 22(7) 473 (1984) https://doi.org/10.1002/mrc.1270220718
Aminopyrazoles. V. Structure assignment of 1H‐pyrazol‐3‐and 5‐amines by means of the 1H NMR δ(4‐H)‐values of their exo‐N‐toluenesulfonyl derivatives
Synthesis of substituted chloroacetylenes from methyl ketones
S. F. Vasilevskii, A. N. Sinyakov, M. S. Shvartsberg and I. L. Kotlyarevskii Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 25(10) 2134 (1976) https://doi.org/10.1007/BF02659533
Reactions of some halocetylenes with sodium amide
M. S. Shavartsberg, S. F. Vasilevskii and A. N. Sinyakov Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 25(10) 2138 (1976) https://doi.org/10.1007/BF02659534
Structure determination of dihydrobis(1-pyrazolyl)borates by proton NMR of potassium salts and nickel(II) chelates
Azole- and ?2-azolinecarbaldehyde oximes and their derivatives
N. I. Shapranova, I. N. Somin and S. G. Kuznetsov Chemistry of Heterocyclic Compounds 9(8) 1018 (1973) https://doi.org/10.1007/BF00471721
Unusual substitution in pyrazolylchloeoacetylene series
M. S. Shwartsberg and S. F. Vasilevskii Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 22(9) 2125 (1973) https://doi.org/10.1007/BF00929433
Pyrazoles XI. The synthesis of 1,1′‐dimethylbipyrazolyls
Pieter B. M. W. M. Timmermans, Arnold P. Uijttewaal and Clarisse L. Habraken Journal of Heterocyclic Chemistry 9(6) 1373 (1972) https://doi.org/10.1002/jhet.5570090632
Etudes RMN en Serie Heterocyclique—VIII: Effet des Dipivalomethanates de Nickel(II), Cobalt(II), Europium(III) et Praseodyme(III) sur les Deplacements Chimiques de quelques Derives du Pyrazoles