Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Nicola Della Ca"'
Autor:
Stefano Bonciolini, Antonio Pulcinella, Matteo Leone, Debora Schiroli, Adrián Luguera Ruiz, Andrea Sorato, Maryne A. J. Dubois, Ranganath Gopalakrishnan, Geraldine Masson, Nicola Della Ca’, Stefano Protti, Maurizio Fagnoni, Eli Zysman-Colman, Magnus Johansson, Timothy Noël
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract In contemporary drug discovery, enhancing the sp3-hybridized character of molecular structures is paramount, necessitating innovative synthetic methods. Herein, we introduce a deoxygenative cross-electrophile coupling technique that pairs ea
Externí odkaz:
https://doaj.org/article/f268aa4aece843bb96f8b5b86625428c
Autor:
Maurizio Chiminelli, Gabriele Scarica, Davide Balestri, Luciano Marchiò, Nicola Della Ca’, Giovanni Maestri
Publikováno v:
Tetrahedron Chem, Vol 8, Iss , Pp 100053- (2023)
The preparation of bridged bicyclooctadienes through the dearomatization of simple arenes is an interesting synthetic tool to access a vast chemical space of elegant molecular architectures from a wide range of simple and cheap building blocks. Howev
Externí odkaz:
https://doaj.org/article/3fdd39522ad84149bf7f6611cad39fd1
Publikováno v:
Catalysts, Vol 13, Iss 6, p 1025 (2023)
This short review is aimed at giving an overview of catalytic carbonylative double cyclization reactions, which are processes in which suitable organic substrates and carbon monoxide are sequentially activated by a promoting a catalyst to form two ne
Externí odkaz:
https://doaj.org/article/973ac9aef9ed4fcbabfeeb0a601084a3
Autor:
Raffaella Mancuso, Ida Ziccarelli, Adele Chimento, Nadia Marino, Nicola Della Ca’, Rosa Sirianni, Vincenzo Pezzi, Bartolo Gabriele
Publikováno v:
iScience, Vol 3, Iss , Pp 279-288 (2018)
Summary: The development of efficient synthetic strategies for the discovery of novel antitumor molecules is a major goal in current research. In this context, we report here a catalytic double cyclization process leading to bicyclic heterocycles wit
Externí odkaz:
https://doaj.org/article/541a620a53e64cafa050afabbe513bb1
Autor:
Vinayak Botla, Aleksandr Voronov, Elena Motti, Carla Carfagna, Raffaella Mancuso, Bartolo Gabriele, Nicola Della Ca’
Publikováno v:
Catalysts, Vol 11, Iss 8, p 918 (2021)
The abundant and inexpensive carbon monoxide (CO) is widely exploited as a C1 source for the synthesis of both fine and bulk chemicals. In this context, photochemical carbonylation reactions have emerged as a powerful tool for the sustainable synthes
Externí odkaz:
https://doaj.org/article/56b030a2290f4e1592331e9cdfb47eee
Autor:
Nicola Della Ca’
Publikováno v:
Catalysts, Vol 11, Iss 5, p 588 (2021)
Palladium is probably the most versatile and exploited transition metal in catalysis due to its capability to promote a myriad of organic transformations both at laboratory and industrial scales (alkylation, arylation, cyclization, hydrogenation, oxi
Externí odkaz:
https://doaj.org/article/be6b588855eb4c7f8a9e7611b442d158
Autor:
Raffaella Mancuso, Ida Ziccarelli, Matteo Brindisi, Cosimo D. Altomare, Luca Frattaruolo, Aurelia Falcicchio, Nicola Della Ca’, Anna Rita Cappello, Bartolo Gabriele
Publikováno v:
Catalysts, Vol 11, Iss 2, p 227 (2021)
We report a stereoselective, multicomponent catalytic carbonylative approach to a new class of α,β-unsaturated γ-lactam derivatives with potential biological activity, that are, alkyl (Z)-2-(2-oxopyrrolidin-3-ylidene)acetates. Our method is based
Externí odkaz:
https://doaj.org/article/a96d16ce84834474ab2477934022af37
Autor:
Alessandra Casnati, Aleksandr Voronov, Damiano Giuseppe Ferrari, Raffaella Mancuso, Bartolo Gabriele, Elena Motti, Nicola Della Ca’
Publikováno v:
Catalysts, Vol 10, Iss 2, p 176 (2020)
The hydroamination reaction is a convenient alternative strategy for the formation of C−N bonds. Herein, we report a new versatile and convenient protocol for the hydroamination of arylacetylenes with anilines using palladium iodide in the absence
Externí odkaz:
https://doaj.org/article/5f2ae3dcd1c448b889bb062f08af1f10
Autor:
Raffaella Mancuso, Rossana Miliè, Ida Ziccarelli, Mariangela Novello, Nicola Della Ca’, Bartolo Gabriele
Publikováno v:
Molbank, Vol 2018, Iss 3, p M1017 (2018)
(S)-4-Isopropyl-5,5-diphenyloxazolidin-2-one has been synthesized for the first time by the enantiospecific oxidative carbonylation of commercially available (S)-2-amino-3-methyl-1,1-diphenylbutan-1-ol. The cyclocarbonylation reaction was carried out
Externí odkaz:
https://doaj.org/article/a6bc78a10f6844199d3815a8259eb7c0
Publikováno v:
Molbank, Vol 2018, Iss 1, p M988 (2018)
The title compound—cis,exo-1,2,3,4,4a,13b-hexahydro-1,4-methano-5-isopropoxy-9H-tribenzo[b,f]azepine—was synthesized in 83% isolated yield by a palladium-catalyzed one-pot strategy from 1-iodo-2-isopropoxybenzene and ortho-bromoaniline. The azepi
Externí odkaz:
https://doaj.org/article/0bedfceae6b54e97b8cde5e02fd8c136