Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Riccardo, Pedrazzani"'
Autor:
Riccardo Pedrazzani, Angela Pintus, Roberta De Ventura, Marianna Marchini, Paola Ceroni, Carlos Silva López, Magda Monari, Marco Bandini
Publikováno v:
ACS Organic & Inorganic Au, Vol 2, Iss 3, Pp 229-235 (2022)
Externí odkaz:
https://doaj.org/article/99e8bcd8d314407eb65095994c4219c7
Autor:
Dario Corbisiero, Tommaso Fantoni, Lucia Ferrazzano, Giulia Martelli, Paolo Cantelmi, Alexia Mattellone, Chiara Palladino, Magda Monari, Riccardo Pedrazzani, Alessandra Tolomelli, Walter Cabri
Publikováno v:
ACS Omega. 7:26919-26927
The enantioselective 1,3-dipolar cycloaddition of nitrones and arylpropionaldehydes to generate highly functionalized scaffolds for application in drug discovery was herein investigated. The use of a second-generation MacMillan catalyst as hydrochlor
Autor:
Simone Battaglioli, Giulio Bertuzzi, Riccardo Pedrazzani, Jessica Benetti, Giovanni Valenti, Marco Montalti, Magda Monari, Marco Bandini
Publikováno v:
Advanced Synthesis & Catalysis. 364:720-725
A dehydrogenative functionalization of styryl carbon-carbon double bonds with triflamide is described via dual visible-light photoredox/cobaloxime catalysis. A range of allylic triflamides (20 examples) were isolated in moderate to good yields (up to
Autor:
Riccardo Pedrazzani, Emanuele Pinosa, Giulio Bertuzzi, Magda Monari, Samuel Lauzon, Thierry Ollevier, Marco Bandini
A new [Au(I)] catalyzed intramolecular hydrocarboxylation of allenes is presented as a valuable synthetic route to oxazino-indolones. The use of 3,5-(CF3)2–C6H3–ImPyAuSbF6 as the optimal catalyst (5 mol%) was necessary to guarantee (i) wide toler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b3a9281abe0d9b338790491a1e7443b
https://hdl.handle.net/11585/900627
https://hdl.handle.net/11585/900627
Autor:
Lorenzo, Lombardi, Alessandro, Cerveri, Leonardo, Ceccon, Riccardo, Pedrazzani, Magda, Monari, Giulio, Bertuzzi, Marco, Bandini
Publikováno v:
Chemical communications (Cambridge, England). 58(25)
A carboxylative Ni-catalyzed tandem C-C σ-bond activation of cyclobutanones followed by CO
Autor:
Lorenzo Di Terlizzi, Simone Scaringi, Carlotta Raviola, Riccardo Pedrazzani, Marco Bandini, Maurizio Fagnoni, Stefano Protti
The preparation of symmetrical (hetero)biaryls via arylazo sulfones has been successfully carried out upon visible light irradiation in the presence of PPh3AuCl as the catalyst. The present protocol led to the efficient synthesis of a wide range of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f6ae0da11522aca42493e69c6d91c1a
https://hdl.handle.net/11585/891403
https://hdl.handle.net/11585/891403
Autor:
Lorenzo Lombardi, Alessandro Cerveri, Leonardo Ceccon, Riccardo Pedrazzani, Magda Monari, Giulio Bertuzzi, Marco Bandini
A carboxylative Ni-catalyzed tandem C-C σ-bond activation of cyclobutanones followed by CO2-electrophilic trapping is documented as a direct route to synthetically valuable 3-indanone-1-acetic acids. The protocol shows an adequate functional group t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2647cf759166b19f4809d9cd896f8559
https://hdl.handle.net/11585/889135
https://hdl.handle.net/11585/889135
New chiral BINOL-based phosphate counterions have been synthesized, fully characterized, and employed in the enantioselective gold-catalyzed dearomatization of -naphthols with allenamides. A range of densely functionalized C1-allylated naphthaleno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ad4498fb738bdcb9fe93c230b68ae6b
http://hdl.handle.net/11585/817850
http://hdl.handle.net/11585/817850
Autor:
Riccardo Giovanelli, Alessandro Cerveri, Riccardo Pedrazzani, Magda Monari, Carlos Silva López, Davide Sella, Marco Bandini, Olalla Nieto Faza
A novel asymmetric nickel-based procedure has been developed in which CO2 fixation is achieved as a second step of a truncated Heck coupling. For this, a new chiral ligand has been prepared and shown to achieve enantiomeric excesses up to 99 %. The o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5440e17c7f8e011a95665b25543a704d
https://hdl.handle.net/11585/821298
https://hdl.handle.net/11585/821298
Autor:
Marco Bandini, Carlos Silva López, Juzeng An, Riccardo Pedrazzani, Magda Monari, Marta Marin-Luna
A novel gold(i)-catalyzed protocol for the synthesis of 4H-1,3-dioxin-3-ones is presented. The protocol exploits a metal induced cascade sequence involving a [3,3]-sigmatropic rearrangement followed by regioselective O-annulation reactions. A wide ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd8673725273ead1390fac305cfb3334
https://hdl.handle.net/11585/768223
https://hdl.handle.net/11585/768223