Novel Purine Chemotypes with Activity against Plasmodium falciparum and Trypanosoma cruzi von Martinez-Peinado, Nieves, Lorente-Macias, Alvaro, Garcia-Salguero, Alejandro, Cortes-Serra, Nuria, Fenollar-Collado, Angel, Ros-Lucas, Albert, Gascon, Joaquim, Pinazo, Maria-Jesus, Molina, Ignacio J., Unciti-Broceta, Asier, Diaz-Mochon, Juan J., de las Infantas y Villatoro, Maria J. Pineda, Izquierdo, Luis, Alonso-Padilla, Julio

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Amide-controlled, one-pot synthesis of tri-substituted purines generates structural diversity and analogues with trypanocidal activity von Pineda de las Infantas y Villatoro, Maria J., Unciti-Broceta, Juan D., Contreras-Montoya, Rafael, Garcia-Salcedo, Jose A., Gallo Mezo, Miguel A., Unciti-Broceta, Asier, Diaz-Mochon, Juan J.

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A New Synthetic Approach to Pyrazolo[3,4-c]-1,2,5-oxadiazoles von Baraldi, Pier Giovanni, Pineda de las Infantas, Maria J., Manfredini, Stefano, Romagnoli, Romeo

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A New Synthetic Approach to Indazole Synthesis von Baraldi, Pier Giovanni, Cacciari, Barbara, Spalluto, Giampiero, Romagnoli, Romeo, Braccioli, Giovanni, Pineda de las Infantas, Maria J.

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Symmetric 4,6-dialkyl/arylamino-5-nitropyrimidines: theoretical explanation of why aminolysis of alkoxy groups is favoured over chlorine aminolysis in nitro-activated pyrimidines von Gómez, Laura Córdoba, Lorente-Macias, Alvaro, Pineda de las Infantas y Villatoro, María José, Garzón-Ruiz, Andrés, Diaz-Mochon, Juan J

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Identification of compounds with activity against Trypanosoma cruzi within a collection of synthetic nucleoside analogs von Barnadas-Carceller, Berta, Martinez-Peinado, Nieves, Gómez, Laura Córdoba, Ros-Lucas, Albert, Gabaldón-Figueira, Juan Carlos, Diaz-Mochon, Juan J, Gascon, Joaquim, Molina, Ignacio J, Pineda de Las Infantas Y Villatoro, María José, Alonso-Padilla, Julio

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1H and 13C assignments of 6‐, 8‐, 9‐ substituted purines von Lorente‐Macías, Álvaro, Benítez‐Quesada, Manuel, Molina, Ignacio J., Unciti‐Broceta, Asier, Díaz‐Mochón, Juan José, Pineda de las Infantas Villatoro, María José

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Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives:  Potent and Selective A2A Adenosine Antagonists von Baraldi, Pier Giovanni, Cacciari, Barbara, Spalluto, Giampiero, Pineda de las Infantas y Villatoro, Maria José, Zocchi, Cristina, Dionisotti, Silvio, Ongini, Ennio

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Synthesis and Biological Activity of a New Series of N6-Arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-Carboxamido Derivatives of Adenosine-5‘-N-ethyluronamide as A1 and A3... von BARALDI, Pier Giovanni, CACCIARI, Barbara, PINEDA DE LAS INFANTAS, Maria José, ROMAGNOLI, Romeo, SPALLUTO, Giampiero, VOLPINI, Rosaria, COSTANZI, Stefano, VITTORI, Sauro, CRISTALLI, Gloria, MELMAN, Neli, PARK, Kyung-Sun, JI, Xiao-duo, JACOBSON, Kenneth A.

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