An overview of stereoselective synthesis of α-aminophosphonic acids and derivatives M Ordóñez, H Rojas-Cabrera, C Cativiela Tetrahedron 65 (1), 17-49, 2009 | 320 | 2009 |
Stereoselective synthesis of γ-amino acids M Ordonez, C Cativiela Tetrahedron: Asymmetry 18 (1), 3-99, 2007 | 254 | 2007 |
Recent progress on the stereoselective synthesis of cyclic quaternary α-amino acids C Cativiela, M Ordóñez Tetrahedron: Asymmetry 20 (1), 1-63, 2009 | 243 | 2009 |
Synthesis of quaternary α-aminophosphonic acids M Ordonez, FJ Sayago, C Cativiela Tetrahedron 68 (32), 6369-6412, 2012 | 113 | 2012 |
An update on the stereoselective synthesis of α-aminophosphonic acids and derivatives M Ordonez, JL Viveros-Ceballos, C Cativiela, FJ Sayago Tetrahedron 71 (12), 1745-1784, 2015 | 107 | 2015 |
An update on the stereoselective synthesis of γ-amino acids M Ordóñez, C Cativiela, I Romero-Estudillo Tetrahedron: Asymmetry 27 (20-21), 999-1055, 2016 | 84 | 2016 |
Stereoselective synthesis of α-aminophosphonic acids analogs of the 20 proteinogenic α-amino acids M Ordonez, J Luis Viveros-Ceballos, C Cativiela, A Arizpe Current Organic Synthesis 9 (3), 310-341, 2012 | 76 | 2012 |
Practical and high stereoselective synthesis of 3-(arylmethylene) isoindolin-1-ones from 2-formylbenzoic acid MA Reyes-González, A Zamudio-Medina, M Ordóñez Tetrahedron Letters 53 (43), 5756-5758, 2012 | 59 | 2012 |
Stereoselective synthesis of acyclic α, α-disubstituted α-amino acids derivatives from amino acids templates C Cativiela, M Ordóñez, JL Viveros-Ceballos Tetrahedron 76 (4), 130875, 2020 | 47 | 2020 |
One-pot three-component highly diastereoselective synthesis of isoindolin-1-one-3-phosphonates under solvent and catalyst free-conditions JL Viveros-Ceballos, C Cativiela, M Ordóñez Tetrahedron: Asymmetry 22 (13), 1479-1484, 2011 | 44 | 2011 |
Enantioselective Diels-Alder reactions catalyzed by chiral magnesium lewis acids prepared from hydroxysulfoxides M Ordoñez, V Guerrero-de La Rosa, V Labastida, JM Llera Tetrahedron: Asymmetry 7 (9), 2675-2686, 1996 | 44 | 1996 |
000Synthesis of new α-aminophosphonates: Evaluation as anti-inflammatory agents and QSAR studies I Romero-Estudillo, JL Viveros-Ceballos, O Cazares-Carreño, ... Bioorganic & Medicinal Chemistry 27 (12), 2376-2386, 2019 | 39 | 2019 |
Preparation of (R)-and (S)-γ-amino-β-hydroxypropylphosphonic acid from glycine M Ordóñez, A González-Morales, C Ruı́z, R De la Cruz-Cordero, ... Tetrahedron: Asymmetry 14 (13), 1775-1779, 2003 | 37 | 2003 |
Practical and efficient synthesis of α-aminophosphonic acids containing 1, 2, 3, 4-tetrahydroquinoline or 1, 2, 3, 4-tetrahydroisoquinoline heterocycles M Ordóñez, A Arizpe, FJ Sayago, AI Jiménez, C Cativiela Molecules 21 (9), 1140, 2016 | 36 | 2016 |
A convenient method for the preparation of chiral phosphonoacetamides and their Horner–Wadsworth–Emmons reaction M Ordonez, E Hernández-Fernández, M Montiel-Perez, R Bautista, ... Tetrahedron: Asymmetry 18 (20), 2427-2436, 2007 | 35 | 2007 |
Synthesis, biological activity and molecular modelling studies of shikimic acid derivatives as inhibitors of the shikimate dehydrogenase enzyme of Escherichia coli DC Díaz-Quiroz, CS Cardona-Félix, JL Viveros-Ceballos, ... Journal of enzyme inhibition and medicinal chemistry 33 (1), 397-404, 2018 | 34 | 2018 |
Phenylphosphonic acid as efficient and recyclable catalyst in the synthesis of α-aminophosphonates under solvent-free conditions M Bedolla-Medrano, E Hernandez-Fernandez, M Ordonez Synlett 25 (08), 1145-1149, 2014 | 34 | 2014 |
Phenylboronic acid as efficient and eco-friendly catalyst for the one-pot, three-component synthesis of α-aminophosphonates under solvent-free conditions GD Tibhe, M Bedolla-Medrano, C Cativiela, M Ordonez Synlett 23 (13), 1931-1936, 2012 | 34 | 2012 |
An easy approach for the synthesis of N-substituted isoindolin-1-ones M Ordonez, GD Tibhe, A Zamudio-Medina, JL Viveros-Ceballos Synthesis 44 (04), 569-574, 2012 | 33 | 2012 |
Synthesis of Aldehydes from Oxiranes Using Silica Gel as Reagent C Lemini, M Ordoñez, J Pérez-Flores, R Cruz-Almanza Synthetic Communications 25, 2695-2702, 0 | 33* | |