Italian chemists' contributions to named reactions in organic synthesis: an historical perspective von Papeo, Gianluca, Pulici, Maurizio

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novel method based on click chemistry, which overcomes limitations of cell cycle analysis by classical determination of BrdU incorporation, allowing multiplex antibody staining von Cappella, Paolo, Gasparri, Fabio, Pulici, Maurizio, Moll, Jürgen

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From polymer to small organic molecules: a tight relationship between radical chemistry and solid-phase organic synthesis von Mirizzi, Danilo, Pulici, Maurizio

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Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining von Cappella, Paolo, Gasparri, Fabio, Pulici, Maurizio, Moll, Jürgen

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Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction von Brunelli, Francesca, Quartieri, Francesca, Miletto, Ivana, Pulici, Maurizio, Papeo, Gianluca, Tron, Gian Cesare

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Cover Feature: Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction (Chem. Eur. J. 50/20... von Brunelli, Francesca, Quartieri, Francesca, Miletto, Ivana, Pulici, Maurizio, Papeo, Gianluca, Tron, Gian Cesare

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Pestalotiopsins A and B:  New Caryophyllenes from an Endophytic Fungus of Taxus brevifolia von Pulici, Maurizio, Sugawara, Fumio, Koshino, Hiroyuki, Uzawa, Jun, Yoshida, Shigeo, Lobkovsky, Emil, Clardy, Jon

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From “Click” to “Fenton” chemistry for 5‐bromo‐2′‐deoxyuridine determination von Cappella, Paolo, Giansanti, Vincenzo, Pulici, Maurizio, Gasparri, Fabio

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Traceless solid-phase synthesis of 2-amino-5-alkylidene-thiazol-4-ones von Pulici, Maurizio, Quartieri, Francesca

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Abstract 1615: NMS-812, a novel potent PERK inhibitor that also inhibits GCN2, exhibits strong anti-tumor activity as single agent and in combination in preclinical models von Perrera, Claudia, Pulici, Maurizio, Banfi, Patrizia, Avanzi, Nilla, Carenzi, Davide, Casero, Daniele, Ciavolella, Antonella, Gianellini, Laura, Gasparri, Fabio, Saturno, Grazia, Valsasina, Barbara, Ardini, Elena, Montagnoli, Alessia, Galvani, Arturo P., Isacchi, Antonella

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Application of Click Chemistry Conditions for 5‐Bromo‐2′‐Deoxyuridine Determination Through Fenton and Related Reactions von Cappella, Paolo, Pulici, Maurizio, Gasparri, Fabio

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Abstract 5163: Characterization of NMS-E194, a selective and potent PERK inhibitor with efficacy in the KMS-11 multiple myeloma von Perrera, Claudia, Pulici, Maurizio, Carenzi, Davide, Motto, Ilaria, Fasolini, Marina, Casale, Elena, Depaolini, Stefania Re, Rizzi, Simona, Asa, Daniela, Roletto, Fulvia, Bindi, Simona, Casero, Daniele, Banfi, Patrizia, Ardini, Elena, Amboldi, Nadia, Ballinari, Dario, Gasparri, Fabio, Cribioli, Sabrina, Mancini, Laura, Ciomei, Marina, Donati, Daniele, Felder, Eduard, Galvani, Arturo, Isacchi, Antonella, Valsasina, Barbara

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3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 1. Lead Finding von Pevarello, Paolo, Brasca, Maria Gabriella, Amici, Raffaella, Orsini, Paolo, Traquandi, Gabriella, Corti, Luca, Piutti, Claudia, Sansonna, Pietro, Villa, Manuela, Pierce, Betsy S, Pulici, Maurizio, Giordano, Patrizia, Martina, Katia, Fritzen, Edward L, Nugent, Richard A, Casale, Elena, Cameron, Alexander, Ciomei, Marina, Roletto, Fulvia, Isacchi, Antonella, Fogliatto, GianPaolo, Pesenti, Enrico, Pastori, Wilma, Marsiglio, Aurelio, Leach, Karen L, Clare, Paula M, Fiorentini, Francesco, Varasi, Mario, Vulpetti, Anna, Warpehoski, Martha A

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Optimization of Diarylthiazole B-Raf Inhibitors: Identification of a Compound Endowed with High Oral Antitumor Activity, Mitigated hERG Inhibition, and Low Paradoxical Effect von Pulici, Maurizio, Traquandi, Gabriella, Marchionni, Chiara, Modugno, Michele, Lupi, Rosita, Amboldi, Nadia, Casale, Elena, Colombo, Nicoletta, Corti, Luca, Fasolini, Marina, Gasparri, Fabio, Pastori, Wilma, Scolaro, Alessandra, Donati, Daniele, Felder, Eduard, Galvani, Arturo, Isacchi, Antonella, Pesenti, Enrico, Ciomei, Marina

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Thieno[3,2- c]pyrazoles: A novel class of Aurora inhibitors with favorable antitumor activity von Bindi, Simona, Fancelli, Daniele, Alli, Cristina, Berta, Daniela, Bertrand, Jay A., Cameron, Alexander D., Cappella, Paolo, Carpinelli, Patrizia, Cervi, Giovanni, Croci, Valter, D’Anello, Matteo, Forte, Barbara, Laura Giorgini, M., Marsiglio, Aurelio, Moll, Juergen, Pesenti, Enrico, Pittalà, Valeria, Pulici, Maurizio, Riccardi-Sirtori, Federico, Roletto, Fulvia, Soncini, Chiara, Storici, Paola, Varasi, Mario, Volpi, Daniele, Zugnoni, Paola, Vianello, Paola

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1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis von Cesarini, Sara, Colombo, Nicoletta, Pulici, Maurizio, Felder, Eduard R., Brill, Wolfgang K.-D.

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Abstract 3754: Characterization of NMS-P285, a new highly selective and potent BRAF inhibitor von Pulici, Maurizio, Amboldi, Nadia, Pastori, Wilma, Marchionni, Chiara, Traquandi, Gabriella, Cribioli, Sabrina, Lupi, Rosita, Modugno, Michele, Casale, Elena, Scolaro, Alessandra, Felder, Eduard, Donati, Daniele, Isacchi, Antonella, Pesenti, Enrico, Galvani, Arturo, Ciomei, Marina

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A cobalt-phosphine complex as mediator in the formation of carbon-carbon bonds von Orsini, Fulvia, Pelizzoni, Francesca, Pulici, Maurizio, Vallarino, Lidia M

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Amylase induction activity of fluorescein labeled gibberellin in barley aleurone protoplasts von Pulici, Maurizio, Asami, Tadao, Robertson, Masumi, Seto, Hideharu, Yoshida, Shigeo

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Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining von Cappella, Paolo, Gasparri, Fabio, Pulici, Maurizio, Moll, Jürgen

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