| Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives: Potent and Selective A2A Adenosine Antagonists PG Baraldi, B Cacciari, G Spalluto, MJ Pineda de las Infantas y Villatoro, ... Journal of medicinal chemistry 39 (5), 1164-1171, 1996 | 143 | 1996 |
| Synthesis and Biological Activity of a New Series of N 6-Arylcarbamoyl, 2-(Ar) alkynyl-N 6-arylcarbamoyl, and N 6-Carboxamido Derivatives of Adenosine-5 ‘-N-ethyluronamide as … PG Baraldi, B Cacciari, MJ Pineda de Las Infantas, R Romagnoli, ... Journal of Medicinal Chemistry 41 (17), 3174-3185, 1998 | 114 | 1998 |
| Design, synthesis, and biological activity of hybrid compounds between uramustine and DNA minor groove binder distamycin A PG Baraldi, R Romagnoli, AE Guadix, MJ Pineda de las Infantas, ... Journal of medicinal chemistry 45 (17), 3630-3638, 2002 | 82 | 2002 |
| Regioselective One-Pot Synthesis of 9-Alkyl-6-chloropyrido[3,2-e][1,2,4]triazolo[4,3-a]pyrazines. Reactivity of Aliphatic and Aromatic Hydrazides A Unciti-Broceta, MJ Pineda-de-las-Infantas, JJ Díaz-Mochón, ... the Journal of Organic chemistry 70 (7), 2878-2880, 2005 | 30 | 2005 |
| Synthesis and Biological Evaluation of Novel N6-[4-(Substituted)sulfonamidophenylcarbamoyl]adenosine-5‘-uronamides as A3 Adenosine Receptor Agonists PG Baraldi, F Fruttarolo, MA Tabrizi, R Romagnoli, D Preti, A Bovero, ... Journal of medicinal chemistry 47 (22), 5535-5540, 2004 | 28 | 2004 |
| An efficient one-pot synthesis of 6-alkoxy-8, 9-dialkylpurines via reaction of 5-amino-4-chloro-6-alkylaminopyrimidines with N, N-dimethylalkaneamides and alkoxide ions PG Baraldi, AU Broceta, MJP De Las Infantas, JJD Mochun, A Espinosa, ... Tetrahedron 58 (38), 7607-7611, 2002 | 26 | 2002 |
| Reduction of Different Electron‐Poor N‐Heteroarylhydrazines in Strong Basic Conditions A Unciti‐Broceta, MJ Pineda de las Infantas, MA Gallo, A Espinosa Chemistry–A European Journal 13 (6), 1754-1762, 2007 | 19 | 2007 |
| Synthesis of 6, 8, 9 poly-substituted purine analogue libraries as pro-apoptotic inducers of human leukemic lymphocytes and DAPK-1 inhibitors MJP De Las Infantas, S Torres-Rusillo, JD Unciti-Broceta, ... Organic & Biomolecular Chemistry 13 (18), 5224-5234, 2015 | 16 | 2015 |
| A mild one-pot synthesis of thieno [3, 4-c] pyrazoles and their conversion into pyrazole analogs of o-quinodimethane PG Baraldi, H El-Kashef, S Manfredini, MJP de las Infantas, R Romagnoli, ... Synthesis 1998 (09), 1331-1334, 1998 | 16 | 1998 |
| Amide-controlled, one-pot synthesis of tri-substituted purines generates structural diversity and analogues with trypanocidal activity MJ Pineda de las Infantas y Villatoro, JD Unciti-Broceta, ... Scientific Reports 5 (1), 9139, 2015 | 12 | 2015 |
| Novel Purine Chemotypes with Activity against Plasmodium falciparum and Trypanosoma cruzi N Martinez-Peinado, Á Lorente-Macías, A García-Salguero, ... Pharmaceuticals 14 (7), 638, 2021 | 7 | 2021 |
| Synthesis of 9-alkyl-6-amino[1,2,4]triazolo[3,4-c]-5-azaquinoxalines. Mild and effective SNAr amination of highly electron poor heterocycles MJPI Asier Unciti Broceta Tetrahedron Letters 51, 2262, 2010 | 7 | 2010 |
| Anew synthetic approach to pyrazolo [3,4-c]-1,2,5-oxadiazoles PB M.José Pineda de las Infantas Synthesis 1, 72, 2000 | 6* | 2000 |
| Identification of compounds with activity against Trypanosoma cruzi within a collection of synthetic nucleoside analogs B Barnadas-Carceller, N Martinez-Peinado, LC Gómez, A Ros-Lucas, ... Frontiers in Cellular and Infection Microbiology 12, 1067461, 2023 | 4 | 2023 |
| 1H and 13C assignments of 6‐, 8‐, 9‐substituted purines Á Lorente-Macías, M Benítez-Quesada, IJ Molina, A Unciti-Broceta, ... Magnetic Resonance in Chemistry, 2018 | 4 | 2018 |
| Synthesis and screening of 6‐alkoxy purine analogs as cell type‐selective apoptotic inducers in Jurkat cells Á Lorente‐Macías, I Iañez, MC Jiménez‐López, M Benítez‐Quesada, ... Archiv der Pharmazie 354 (10), 2100095, 2021 | 3 | 2021 |
| Synthesis of oxadiazoline and quinazoline derivatives and their biological evaluation as nitric oxide synthase inhibitors MDC M.José Pineda de las Infantas Medicinal Chemistry Research, 2016 | 3 | 2016 |
| Amide-controlled, one-pot synthesis of tri-substituted purines generates structural diversity and analogues with trypanocidal activity. PI y Villatoro, JD Unciti-Broceta, R Contreras-Montoya, JA Garcia-Salcedo, ... Scientific Reports 5, 9139-9139, 2015 | 3 | 2015 |
| Design and Synthesis of 9-Dialkylamino-6-[(1H-1, 2, 3-triazol-4-yl) methoxy]-9H-purines Á Lorente-Macías, JJ Díaz-Mochón, MJP de las Infantas, A Unciti-Broceta | 1 | 2021 |
| NMR and confomational studies of new 5-phenylpyrrole-carboxamide derivatives MDC M.José Pineda de las Infantas Magnetic Resonance in Chemistry 47, 1101, 2009 | 1* | 2009 |
