Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Arianna Sinibaldi"'
Publikováno v:
Asymmetric Organocatalysis. :271-317
Autor:
Antonio Del Vecchio, Arianna Sinibaldi, Valeria Nori, Giuliana Giorgianni, Graziano Di Carmine, Fabio Pesciaioli
Publikováno v:
Chemistry – A European Journal. 28
Autor:
Graziano Di Carmine, Fabio Pesciaioli, Simeng Wang, Arianna Sinibaldi, Giuliana Giorgianni, Christopher M. A. Parlett, Armando Carlone, Carmine D'Agostino
Publikováno v:
ChemCatChem. 14
Autor:
Antonio Del Vecchio, Arianna Sinibaldi, Valeria Nori, Giuliana Giorgianni, Graziano Di Carmine, Fabio Pesciaioli
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(49)
Synergistic catalysis offers the unique possibility of simultaneous activation of both the nucleophile and the electrophile in a reaction. A requirement for this strategy is the stability of the active species towards the reaction conditions and the
Design of Experiments (DoE) is extensively and routinely used in industry; however, in recent decades, it has gained increasing interest from academia in organic synthesis. The use of chemometrics is an attractive strategy to find the real optimum in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4691d39aefa967ad88b3aea6972afb66
http://hdl.handle.net/11697/175773
http://hdl.handle.net/11697/175773
Autor:
Valeria Nori, Arianna Sinibaldi, Giuliana Giorgianni, Fabio Pesciaioli, Francesca Di Donato, Emanuele Cocco, Alessandra Biancolillo, Aitor Landa, Armando Carlone
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(24)
The development of an enantioselective enamine-catalysed addition of masked acetaldehyde to nitroalkenes via a rational approach helped to move away from the use of chloroform. The presented research allows the use of water as a reaction medium, ther
Autor:
Fabio Pesciaioli, Francesco Fini, Francesca Della Penna, Arianna Sinibaldi, Marco Ponzetti, Silvia Marchesan, Armando Carlone, Andrea Baschieri
Self-assembling minimalistic peptides embedded with an organocatalytic moiety were designed. By controlling the formation of fibrils via external intervention, it was shown that the activation is accelerated when the organocatalyst is in its supramol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::179dea0be3ddeb6ab3677c6ef4f561b7
https://hdl.handle.net/11368/2997541
https://hdl.handle.net/11368/2997541
Publikováno v:
Catalysts, Vol 12, Iss 5, p 5 (2022)
In the last two decades, boron-based catalysis has been gaining increasing traction in the field of organic synthesis. The use of halogenated triarylboranes as main group Lewis acid catalysts is an attractive strategy. It has been applied in a growin
Autor:
Francesca Della Penna, Marco Ponzetti, Arianna Sinibaldi, Silvia Marchesan, Andrea Baschieri, Armando Carlone, Fabio Pesciaioli, Francesco Fini
Publikováno v:
European Journal of Organic Chemistry. 2021:5387-5387