Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alessandro Castrogiovanni"'
Autor:
Antonio Cardinale, Alessandro Castrogiovanni, Theophile Gaudin, Joppe Geluykens, Teodoro Laino, Matteo Manica, Daniel Probst, Philippe Schwaller, Aleksandros Sobczyk, Alessandra Toniato, Alain C. Vaucher, Heiko Wolf, Federico Zipoli
Publikováno v:
CHIMIA, Vol 77, Iss 7/8 (2023)
The RXN for Chemistry project, initiated by IBM Research Europe – Zurich in 2017, aimed to develop a series of digital assets using machine learning techniques to promote the use of data-driven methodologies in synthetic organic chemistry. This res
Externí odkaz:
https://doaj.org/article/a7d5d4b484f54709884821f7a8e58eba
Autor:
Daniel Probst, Matteo Manica, Yves Gaetan Nana Teukam, Alessandro Castrogiovanni, Federico Paratore, Teodoro Laino
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
As of now, only rule-based systems support retrosynthetic planning using biocatalysis, while initial data-driven approaches are limited to forward predictions. Here, the authors extend the data-driven forward reaction as well as retrosynthetic pathwa
Externí odkaz:
https://doaj.org/article/f83b344da0d24f9f98411b6ccdb3ed15
Autor:
Daniel Moser, Alessandro Castrogiovanni, Dominik Lotter, Reto M. Witzig, Vincent C. Fäseke, Felix C. Raps, Christof Sparr
Publikováno v:
CHIMIA, Vol 74, Iss 9, Pp 699-703 (2020)
Aldol reactions belong to the most important methods for carbon–carbon bond formation and are also involved in one of the most astonishing biosynthetic processes: the biosynthesis of polyketides governed by an extraordinarily sophisticated enzymati
Externí odkaz:
https://doaj.org/article/88f8f1d28f8f498a939675190ff03f3a
Publikováno v:
ACS Central Science, Vol 4, Iss 5, Pp 656-660 (2018)
Externí odkaz:
https://doaj.org/article/4a9207c09f06459898e04bfa42ded153
Autor:
Daniel Probst, Matteo Manica, Yves Gaetan Nana Teukam, Alessandro Castrogiovanni, Federico Paratore, Teodoro Laino
Publikováno v:
Nature communications. 13(1)
Enzyme catalysts are an integral part of green chemistry strategies towards a more sustainable and resource-efficient chemical synthesis. However, the use of biocatalysed reactions in retrosynthetic planning clashes with the difficulties in predictin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd5c64ebc999eaa8fe4b6d245f8b168
https://pubmed.ncbi.nlm.nih.gov/35181654
https://pubmed.ncbi.nlm.nih.gov/35181654
Autor:
Alessandro Castrogiovanni
Articolo che analizza con un leggero sfondo giuridico, filosofico e storico, l'attuale situazione di crisi pandemica da Covid-19relazionata ai valori dell'Unione Europea ed in particolare a quello di solidarietà.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bb7d49da350c961cb600d60f65f512f
A topologically well-defined atropisomeric teraryl monophosphine ligand system, prepared by a highly stereoselective arene-forming aldol condensation combined with a direct ester-to-anthracene transformation, is described herein. The ligands were eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dc4a4565d3de22275597457463e2a19
Publikováno v:
ACS Catalysis. 8:2981-2988
Owing to their favorable molecular topology, atropisomers represent particularly valuable chiral scaffolds for numerous applications throughout academic research and industry. Nevertheless, whereas various well-established catalyst-controlled methodo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb01422eb209ef4bc5eb75501bfaa8e4
https://doi.org/10.1021/acscatal.7b04337
https://doi.org/10.1021/acscatal.7b04337
Autor:
Christopher B. Larsen, Patrick Herr, Christof Sparr, Xingwei Guo, Alessandro Castrogiovanni, Oliver S. Wenger
Atropisomeric 1,2-naphthylene scaffolds provide access to donor-acceptor compounds with helical oligomer-based bridges, and transient absorption studies revealed a highly unusual dependence of the electron-transfer rate on oligomer length, which is d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f96ca1c95855ad3bdd5c7badbc8100a
https://edoc.unibas.ch/73735/
https://edoc.unibas.ch/73735/