Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andrea Sorato"'
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:
Alessia Ciogli, Andrea Fochetti, Andrea Sorato, Giancarlo Fabrizi, Nunzio Matera, Andrea Mazzanti, Michele Mancinelli
Publikováno v:
Molecules, Vol 28, Iss 13, p 4915 (2023)
The dynamic scenario of di-aryls-pyrano-chromenes was investigated using DFT calculations. The symmetry of the chromene scaffold and the presence of two ortho-substituted aryls substituents can generate two syn/anti diastereoisomers and conformationa
Externí odkaz:
https://doaj.org/article/332d592586ac43f6a811ab04c5151923
Autor:
Mancinelli, Alessia Ciogli, Andrea Fochetti, Andrea Sorato, Giancarlo Fabrizi, Nunzio Matera, Andrea Mazzanti, Michele
Publikováno v:
Molecules; Volume 28; Issue 13; Pages: 4915
The dynamic scenario of di-aryls-pyrano-chromenes was investigated using DFT calculations. The symmetry of the chromene scaffold and the presence of two ortho-substituted aryls substituents can generate two syn/anti diastereoisomers and conformationa
Publikováno v:
Angewandte Chemie-International Edition, 62(3):e202215374. John Wiley and Sons Ltd
Angewandte Chemie, 135(3):e202215374. John Wiley and Sons Ltd
Angewandte Chemie, 135(3):e202215374. John Wiley and Sons Ltd
The ability to construct C(sp3)−C(sp3) bonds from easily accessible reagents is a crucial, yet challenging endeavor for synthetic organic chemists. Herein, we report the realization of such a cross-coupling reaction, which combines N-sulfonyl hydra
Autor:
Chiara Salvitti, Giulia de Petris, Anna Troiani, Marta Managò, Claudio Villani, Alessia Ciogli, Andrea Sorato, Andreina Ricci, Federico Pepi
Publikováno v:
Journal of the American Society for Mass Spectrometry. 33:565-572
Thin films derived by the deposition of charged microdroplets generated in the ESI source of a mass spectrometer act as highly concentrated reaction vessels in which the final products of an ion-molecule reaction can be isolated by their precipitatio
Publikováno v:
Angewandte Chemie (International ed. in English). 62(3)
The ability to construct C(sp
The ability to construct C(sp3)–C(sp3) bonds from easily accessible reagents is a crucial, yet challenging endeavor for synthetic organic chemists. Herein, we report the realization of such a cross-coupling reaction, which combines N-sulfonyl hydra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba0bc3566ce8d7dc571215146579f35
https://doi.org/10.26434/chemrxiv-2022-h91bz
https://doi.org/10.26434/chemrxiv-2022-h91bz
Autor:
Chiara Portolani, Giovanni Centonze, Sara Luciani, Andrea Pellegrini, Paolo Righi, Andrea Mazzanti, Alessia Ciogli, Andrea Sorato, Giorgio Bencivenni
Publikováno v:
Angewandte Chemie. 134
The first catalytic enantioselective and diastereoselective synthesis of atropisomeric hydrazides was achieved using a sequential catalysis protocol. This strategy is based on a one-pot sequence of two organocatalytic cycles featuring the enamine ami