Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Marina Zenzola"'
Autor:
Claudia Carlucci, Luisa Pisano, Giuseppe Romanazzi, Renzo Luisi, Giovanna Parisi, Emanuela Capitanelli, Leonardo Degennaro, Marina Zenzola
Publikováno v:
Pure and Applied Chemistry. 88:631-648
Interest in molecular structures bearing four-membered heterocycles (FMHs) is growing due to the possibility to explore new regions of the chemical space and get new lead molecules. Our interest in the development of divergent synthesis of functional
Publikováno v:
Angewandte Chemie (International Ed. in English)
The transfer of nitrogen atoms is extremely valuable in the preparation of medicinal compounds. Here, a new system for NH transfer is developed to prepare sulfoximines, which are emerging as valuable motifs for drug discovery. This is achieved using
Publikováno v:
The Journal of Organic Chemistry. 80:6391-6399
Sulfoximines are of considerable interest for incorporation into medicinal compounds. A convenient synthesis of N-protected sulfoximines is achieved, under mild conditions, by rhodium-catalyzed transfer of carbamates to sulfoxides. The first examples
Autor:
Renzo Luisi, Carlo Franchini, Solomon Habtemariam, Leonardo Degennaro, Maria Maddalena Cavalluzzi, Giovanni Lentini, Annunziatina Laurino, Marina Zenzola, Rosanna Matucci
Alternative and complementary procedures were adopted for preparing 2-arylazetidine derivatives in moderate to good yields. Preliminary biological evaluation of 2-arylazetidines as ligands of nicotinic acetylcholine receptors allowed to identify chlo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41cbe6ac2b8d933b14e75d44c95715a
http://hdl.handle.net/11365/1189877
http://hdl.handle.net/11365/1189877
Autor:
Leonardo Degennaro, Giuseppe Romanazzi, Sahra St John-Campbell, Renzo Luisi, James A. Bull, Stephen John Chawner, Claudia Carlucci, Arianna Tota, Marina Zenzola
Publikováno v:
Chemical communications (Cambridge, England). 53(2)
Direct synthesis of NH-sulfoximines from sulfides has been achieved through O and NH transfer in the same reaction, occurring with complete selectivity. The reaction is mediated by bisacetoxyiodobenzene under simple conditions and employs inexpensive
Publikováno v:
ChemInform. 47
An extremely useful method for the conversion of variously substituted sulfoxides to sulfoximines using ammonium carbamate as nitrogen source is reported.
Autor:
Giovanna Parisi, Marina Zenzola, Laura Carroccia, Luisa Pisano, Leonardo Degennaro, Flavio Fanelli, Giuseppe Romanazzi, Renzo Luisi
Publikováno v:
ChemInform. 47
Starting from readily available C2-substituted thietane 1-oxides, a straightforward synthesis of new C2,C4-disubstituted thietane 1-oxides has been developed by using a lithiation/electrophilic trapping sequence. The chemical and configurational stab
Autor:
Giovanna Parisi, Laura Carroccia, Renzo Luisi, Leonardo Degennaro, Giuseppe Romanazzi, Flavio Fanelli, Marina Zenzola, Luisa Pisano
Publikováno v:
The Journal of organic chemistry. 80(24)
Starting from readily available C2-substituted thietane 1-oxides, a straightforward synthesis of new C2,C4-disubstituted thietane 1-oxides has been developed by using a lithiation/electrophilic trapping sequence. The chemical and configurational stab
Publikováno v:
ChemInform. 46
Sulfoximines are of considerable interest for incorporation into medicinal compounds. A convenient synthesis of N-protected sulfoximines is achieved, under mild conditions, by rhodium-catalyzed transfer of carbamates to sulfoxides. The first examples
Autor:
Giuseppe Romanazzi, Piero Mastrorilli, Piera Trinchera, Leonardo Degennaro, Luisa Pisano, Marina Zenzola, Rosanna Rizzi, Renzo Luisi, Arianna Giovine, Laura Carroccia
Publikováno v:
ChemInform. 46
This work demonstrates how the directing ability of the azetidine ring could be useful for regioselective ortho-CH functionalization of aryl compounds. Robust polar organometallic (lithiated) intermediates are involved in this synthetic strategy. The