Zobrazeno 1 - 10
of 118
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:
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
Publikováno v:
Molecules, Vol 25, Iss 14, p 3242 (2020)
Indole derivatives are among the most useful and interesting heterocycles employed in drug discovery and medicinal chemistry. In addition, flow chemistry and flow technology are changing the synthetic paradigm in the field of modern synthesis. In thi
Externí odkaz:
https://doaj.org/article/510de896cd614d7abeb8ce0c9274f486
Autor:
Arianna Giovine, Marilena Muraglia, Marco Antonio Florio, Antonio Rosato, Filomena Corbo, Carlo Franchini, Biagia Musio, Leonardo Degennaro, Renzo Luisi
Publikováno v:
Molecules, Vol 19, Iss 8, Pp 11505-11519 (2014)
By using the Suzuki-Miyaura protocol, a simple straightforward synthesis of functionalized 2-arylaziridines has been developed. By means of this synthetic strategy from readily available ortho-, meta- and para-bromophenylaziridines and aryl- or heter
Externí odkaz:
https://doaj.org/article/987bfcdb99f34a30a71561822cf81c17
Publikováno v:
Catalysts, Vol 9, Iss 1, p 75 (2019)
The discovery of alternative fuels that can replace conventional fuels has become the goal of many scientific researches. Biodiesel is produced from vegetable oils through a transesterification reaction that converts triglycerides into fatty acid met
Externí odkaz:
https://doaj.org/article/7c8fd44af21a40cdac3bc8ab44f77a61
Publikováno v:
Arkivoc. 2023:33-49