José Luis Viveros Ceballos

Doctorado en Ciencias, Química, Facultad de Ciencias de la Universidad Autónoma del Estado de Morelos (2014), Mención honorífica.
Profesor- Asociado C
SNI: Nivel I
Línea de Investigación:
Cuerpo Académico: Síntesis Orgánica
2018

15. Díaz-Quiroz, D. C.; Cardona-Félix, C. S.; Viveros-Ceballos, J. L.; Reyes-González, M. A.; Bolívar, F.; Ordoñez, M.; Escalante, A.* Synthesis, Biological Activity and Molecular Modelling Studies of Shikimic Acid Derivatives as Inhibitors of the Shikimate Dehydrogenase Enzyme of Escherichia Coli. J. Enzyme Inhib. Med. Chem. 2018, 33 (1), 397–404. DOI: 10.1080/14756366.2017.1422125

2017

14. Cervera-Villanueva, J. M. J.; Viveros-Ceballos, J. L.; Ordóñez, M*. First Practical Synthesis of Novel 1-Phosphonylated pyrrolo[1,2- a ]Pyrazine Derivatives. Heteroat. Chem. 2017, 28 (5), e21398. DOI: 10.1002/hc.21398

13. Ordóñez, M.*; Viveros-Ceballos, J. L.; Sayago, F. J.; Cativiela, C.* Stereoselective synthesis of α-amino-H-phosphinic acids and derivatives. Synthesis 2017, 49, 987-997. DOI: 10.1055/s-0036-1588617

12. Viveros-Ceballos, J. L.*; Martínez-Toto, E. I.; Eustaquio-Armenta, C.; Cativiela, C.; Ordóñez, M.* First and Highly Stereoselective Synthesis of Both Enantiomers of Octahydroindole-2-Phosphonic Acid (Oic P). European J. Org. Chem. 2017, 2017 (45), 6781–6787. DOI: 10.1002/ejoc.201701330

11. Ordóñez, M.*; Viveros‐Ceballos, J. L.; Estudillo, I. R. Stereoselective Synthesis of α‐Aminophosphonic Acids through Pudovik and Kabachnik‐Fields Reaction. In Amino Acid - New Insights and Roles in Plant and Animal; InTech, 2017. DOI: 10.5772/intechopen.68707

2016

10. Viveros-Ceballos, J.; Ordóñez, M.*; Sayago, F.; Cativiela, C.* Stereoselective Synthesis of α-Amino-C-Phosphinic Acids and Derivatives. Molecules 2016, 21 (9), 1141. DOI: 10.3390/molecules21091141

9. Viveros-Ceballos, J. L.; Ordóñez, M.*; Sayago, F. J.; Jiménez, A. I.; Cativiela, C.* First Synthesis of (R)- and (S)-1, 2, 3, 4-Tetrahydroisoquinoline-3-Phosphonic Acid (Tic P ) Using a Pictet-Spengler Reaction. European J. Org. Chem. 2016, 2016 (15), 2711–2719. DOI: 10.1002/ejoc.201600313

8. Cervera-Villanueva, J. M. J.; Viveros-Ceballos, J. L.; Linzaga-Elizalde, I.; Ordóñez, M.* Practical Synthesis of Novel Phosphonopeptides Containing Aib P. J. Pept. Sci. 2016, 22 (2), 70–75. DOI: 10.1002/psc.2841

7. Ramírez-Marroquín, O. A.; Romero-Estudillo, I.; Viveros-Ceballos, J. L.; Cativiela, C.; Ordóñez, M.* Convenient Synthesis of Cyclic α-Aminophosphonates by Alkylation-Cyclization Reaction of Iminophosphoglycinates Using Phase-Transfer Catalysis. European J. Org. Chem. 2016, 2016 (2), 308–313. DOI: 10.1002/ejoc.201501203

2015

6. Ordóñez, M.*; Viveros-Ceballos, J. L.; Cativiela, C.*; Sayago, F. J. An Update on the Stereoselective Synthesis of α-Aminophosphonic Acids and Derivatives. Tetrahedron 2015, 71 (12), 1745–1784. DOI: 10.1016/j.tet.2015.01.029

5. Viveros-Ceballos, J. L.; Sayago, F. J.; Cativiela, C.*; Ordóñez, M.* First Practical and Efficient Synthesis of 3-Phosphorylated β-Carboline Derivatives Using the Pictet-Spengler Reaction. European J. Org. Chem. 2015, 2015 (5), 1084–1091. DOI: 10.1002/ejoc.201403418

2014

4. Bonilla-Landa, I.; Viveros-Ceballos, J. L.; Ordóñez, M.* Diastereoselective Synthesis of Novel 5-Substituted Morpholine-3-Phosphonic Acids: Further Exploitation of N-Acyliminium Intermediates. Tetrahedron: Asymmetry 2014, 25 (6–7), 485–487. DOI: 10.1016/j.tetasy.2014.02.014

2012

3. Ordóñez, M.*; Tibhe, G. D.; Zamudio-Medina, A.; Viveros-Ceballos, J. L. An Easy Approach for the Synthesis of N-Substituted Isoindolin-1-Ones. Synthesis (Stuttg). 2012, 44 (4), 569–574. DOI: 10.1055/s-0031-1289680

2. Ordonez, M.; Luis Viveros-Ceballos, J.; Cativiela, C.; Arizpe, A. Stereoselective Synthesis of α-Aminophosphonic Acids Analogs of the 20 Proteinogenic α-Amino Acids. Curr. Org. Synth. 2012, 9 (3), 310–341. DOI: 10.2174/157017912801270595

2011

1. Viveros-Ceballos, J. L.; Cativiela, C.; Ordóñez, M.* One-Pot Three-Component Highly Diastereoselective Synthesis of Isoindolin-1-One-3-Phosphonates under Solvent and Catalyst Free-Conditions. Tetrahedron: Asymmetry 2011, 22 (13), 1479–1484. DOI: 10.1016/j.tetasy.2011.08.003