| Swelling and methylene blue adsorption of poly (N, N-dimethylacrylamide-co-2-hydroxyethyl methacrylate) hydrogel AR Hernandez-Martínez, JA Lujan-Montelongo, C Silva-Cuevas, ... Reactive and Functional Polymers 122, 75-84, 2018 | 87 | 2018 |
| Alkyl sulfinates: Formal nucleophiles for synthesizing TosMIC analogs JA Lujan‐Montelongo, AO Estevez, FF Fleming European journal of organic chemistry 2015 (7), 1602-1605, 2015 | 44 | 2015 |
| Lead (II) Removal by poly(N,N-Dimethylacrylamide-Co-2-Hydroxyethyl Methacrylate) AL Ramos-Jacques, JA Lujan-Montelongo, C Silva-Cuevas, ... European Polymer Journal, 2018 | 34 | 2018 |
| New Heck coupling strategies for the synthesis of paullone and dimethyl paullone JG Avila-Zárraga, A Lujan-Montelongo, A Covarrubias-Zúñiga, ... Tetrahedron letters 47 (45), 7987-7989, 2006 | 32 | 2006 |
| Sulfonyl halide synthesis by thiol oxyhalogenation using NBS/NCS - iPrOH C Silva-Cuevas, C Pérez-Arrieta, LA Polindara, JA Lujan-Montelongo Tetrahedron Letters 58, 2017 | 26 | 2017 |
| Synthesis of polysubstituted isoindolinones via radical cyclization of 1, 3-dicarbonyl Ugi-4CR adducts using tetrabutylammonium persulfate and TEMPO A Borja-Miranda, F Valencia-Villegas, JA Lujan-Montelongo, ... The Journal of Organic Chemistry 86 (1), 929-946, 2020 | 19 | 2020 |
| Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines SV Chepyshev, JA Lujan-Montelongo, A Chao, FF Fleming Angewandte Chemie International Edition, 2017 | 19 | 2017 |
| Microwave-assisted C-3 selective oxidative radical alkylation of flavones MV Mijangos, J González-Marrero, LD Miranda, P Vincent-Ruz, ... Organic & Biomolecular Chemistry 10 (15), 2946-2949, 2012 | 19 | 2012 |
| The two faces of sulfinates: illustrating umpolung reactivity A Tapia-Pineda, C Perez-Arrieta, C Silva-Cuevas, E Paleo, ... Journal of Chemical Education 93 (8), 1470-1474, 2016 | 17 | 2016 |
| Palladium (II) catalyzed 5-endo epoxynitrile cyclizations: total syntheses of enokipodins A and B JA Luján-Montelongo, JG Ávila-Zárraga Tetrahedron Letters 51 (17), 2232-2236, 2010 | 14 | 2010 |
| Asmic: an exceptional building block for isocyanide alkylations E Alwedi, JA Lujan-Montelongo, BR Pitta, A Chao, R Cortés-Mejía, ... Organic letters 20 (18), 5910-5913, 2018 | 13 | 2018 |
| Isocyano enones: Addition–cyclization cascade to oxazoles A Chao, JA Lujan-Montelongo, FF Fleming Organic letters 18 (13), 3062-3065, 2016 | 13 | 2016 |
| Asmic Isocyanide‐Nitrile Isomerization‐Alkylations E Alwedi, JA Lujan‐Montelongo, R Cortés‐Mejía, JM del Campo, ... European Journal of Organic Chemistry 2019 (29), 4644-4648, 2019 | 9 | 2019 |
| Highly regioselective enzymatic synthesis of lutein-3-monoesters JA Lujan-Montelongo, HL Mendoza-Figueroa, C Silva-Cuevas, ... Tetrahedron letters 59 (46), 4096-4101, 2018 | 9 | 2018 |
| An expeditious and efficient bromomethylation of thiols: enabling bromomethyl sulfides as useful building blocks C Silva-Cuevas, E Paleo, DF León-Rayo, JA Lujan-Montelongo RSC advances 8 (43), 24654-24659, 2018 | 9 | 2018 |
| Regio and stereo selectivity on the α-aryl-δ-epoxynitrile anionic cyclization reactions: Modulation towards a 5-endo or 4-exo process JG Ávila-Zárraga, A Vazquez-Sanchez, JA Luján-Montelongo Heterocycles 78 (8), 1955, 2009 | 7 | 2009 |
| An efficient synthesis of (+/-)-xanthorrhizol: One pot decyanation and demethylation JA Lujan-Montelongo, A Covarrubias-Zuniga, M Romero-Ortega, ... Letters in Organic Chemistry 5 (6), 470-472, 2008 | 7 | 2008 |
| Metalated Nitriles: SNi and SNi'installation of contiguous quaternary-tertiary and quaternary-quaternary centers JA Lujan-Montelongo, P Lu, W Liu, FF Fleming Chemistry (Weinheim an der Bergstrasse, Germany) 19 (27), 2013 | 6 | 2013 |
| Preparation of 3‐Oxocyclohex‐1‐ene‐1‐carbonitrile JA Lujan‐Montelongo, FF Fleming Organic Syntheses, 229-239, 2013 | 6* | 2013 |
| Iodine and Iodide in Reductive Transformations JA Luján‐Montelongo, JB Mateus‐Ruiz, RM Valdez‐García European Journal of Organic Chemistry 26 (9), e202201156, 2023 | 4 | 2023 |
Fraser FlemingProfessor of Chemistry, Drexel UniversityDirección de correo verificada de drexel.edu
