alpha-Substituted beta-keto esters have been transformed by means of a straightforward procedure into aziridine-1,2-dicarboxylates, which have been efficiently converted into alkenyl aziridine-1,2-dicarboxylates through Wittig olefination reaction. The possibility of aziridine ring elaborations and the presence of an olefin function make these new molecules suitable scaffolds for further derivatisation into potential bioactive targets.

Functionalised Enones as Starting Materials for the Construction of Aziridine Scaffolds / Fioravanti, Stefania; Morreale, Alberto; Pellacani, Lucio; Tardella, Paolo Antonio. - In: MOLECULAR DIVERSITY. - ISSN 1381-1991. - STAMPA. - 6:(2003), pp. 177-180. [10.1023/B:MODI.0000006757.23657.11]

Functionalised Enones as Starting Materials for the Construction of Aziridine Scaffolds

FIORAVANTI, Stefania;MORREALE, Alberto;PELLACANI, Lucio;TARDELLA, Paolo Antonio
2003

Abstract

alpha-Substituted beta-keto esters have been transformed by means of a straightforward procedure into aziridine-1,2-dicarboxylates, which have been efficiently converted into alkenyl aziridine-1,2-dicarboxylates through Wittig olefination reaction. The possibility of aziridine ring elaborations and the presence of an olefin function make these new molecules suitable scaffolds for further derivatisation into potential bioactive targets.
2003
aziridination; carbamates; olefination; scaffold; solution phase
01 Pubblicazione su rivista::01a Articolo in rivista
Functionalised Enones as Starting Materials for the Construction of Aziridine Scaffolds / Fioravanti, Stefania; Morreale, Alberto; Pellacani, Lucio; Tardella, Paolo Antonio. - In: MOLECULAR DIVERSITY. - ISSN 1381-1991. - STAMPA. - 6:(2003), pp. 177-180. [10.1023/B:MODI.0000006757.23657.11]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/364967
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