Zobrazeno 1 - 10
of 239
pro vyhledávání: '"Leonardo Degennaro"'
Autor:
Arianna Tota, Michael Andresini, Marco Colella, Roberta Savina Dibenedetto, Leonardo Degennaro, Renzo Luisi
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1518 (2022)
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (R)-4-methylbenzenesulfonimidate was synthesized via the stereoselective NH-transfer to (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (S)-4-methylbenzenesulfinate. The reaction employed diacetoxyiodobenzene (DIB)
Externí odkaz:
https://doaj.org/article/c468dfa2afa74852b8ccc9f32a60f3a2
Autor:
Pantaleo Musci, Marco Colella, Angela Altomare, Giuseppe Romanazzi, Nadeem S. Sheikh, Leonardo Degennaro, Renzo Luisi
Publikováno v:
Molecules, Vol 27, Iss 9, p 2847 (2022)
In this work it is demonstrated that enantiomerically enriched N-alkyl 2-oxazolinylazetidines undergo exclusive α-lithiation, and that the resulting lithiated intermediate is chemically stable but configurationally labile under the given experimenta
Externí odkaz:
https://doaj.org/article/86aaf622ac46459380b54e57db5175de
Autor:
Marco Colella, Pantaleo Musci, Claudia Carlucci, Samuele Lillini, Mara Tomassetti, Andrea Aramini, Leonardo Degennaro, Renzo Luisi
Publikováno v:
ACS Omega, Vol 3, Iss 11, Pp 14841-14848 (2018)
Externí odkaz:
https://doaj.org/article/6e829e3070a142628b1758f78ec7aafd
Publikováno v:
Arkivoc. 2023:33-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8b4de54fa04140fe59e2182bfe6f85e
https://doi.org/10.24820/ark.5550190.p011.844
https://doi.org/10.24820/ark.5550190.p011.844
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 520-542 (2017)
Microreactor technology and flow chemistry could play an important role in the development of green and sustainable synthetic processes. In this review, some recent relevant examples in the field of flash chemistry, catalysis, hazardous chemistry and
Externí odkaz:
https://doaj.org/article/6a2db4ae816f451fa8595fa5a66b0a13
Autor:
Pantaleo Musci, Marco Colella, Flavio Fanelli, Angela Altomare, Luisa Pisano, Claudia Carlucci, Renzo Luisi, Leonardo Degennaro
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
A new synthetic route to N-alkyl-2-acylazetidines was developed through a highly stereoselective addition of organolithiums to N-alkyl-2-oxazolinylazetidines followed by acidic hydrolysis of the resulting oxazolidine intermediates. This study reveale
Externí odkaz:
https://doaj.org/article/41de264dc36747de80b8f2e2932f053d
Autor:
Giovanni Lentini, Maria Maddalena Cavalluzzi, Leonardo Degennaro, Giuseppe Fracchiolla, Filippo Perna, Antonio Scilimati
Publikováno v:
Molbank, Vol 2019, Iss 1, p M1049 (2019)
A multistep gram-scale synthesis of (S)-ethyl 2-(tert-butoxycarbonylamino)-3-(2-iodo-4,5-methylenedioxyphenyl)propanoate (2) has been developed. The title compound was prepared starting from commercially available l-DOPA which was O- and N-protected
Externí odkaz:
https://doaj.org/article/47db19e9f9de4849b3f04efbfe588dd6
Autor:
Pantaleo Musci, Marco Colella, Michael Andresini, Andrea Aramini, Leonardo Degennaro, Renzo Luisi
Publikováno v:
Chemical Communications. 58:6356-6359
The use of flow technology as an enabling tool for accessing 1-azabicyclo[1.1.0]butanes bearing strained 3-, 4-, and 5-membered O-heterocycles with C3(N-het)–C2(O-het) connectivity is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bfd17828184d1001c29d5651fed65fe
https://doi.org/10.1039/d2cc01641a
https://doi.org/10.1039/d2cc01641a
Autor:
Marco Colella, Pantaleo Musci, Michael Andresini, Mauro Spennacchio, Leonardo Degennaro, Renzo Luisi
Publikováno v:
Organic & Biomolecular Chemistry. 20:4669-4680
This minireview covers the recent relevant literature updates on the use of CH2FI as readily available platform for monofluoromethylation strategies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4c0217705d5500934ea33decf57e0d0
https://doi.org/10.1039/d2ob00670g
https://doi.org/10.1039/d2ob00670g
Publikováno v:
Arkivoc. 2021:141-163
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afbaff9d48a036e4cb8b23e4126a6dd3
https://doi.org/10.24820/ark.5550190.p011.654
https://doi.org/10.24820/ark.5550190.p011.654