Lipophilic saturated and unsaturated L-ascorbyl 5,6-O-diesters from fatty acids are prepared and fully characterized through NMR and MS spectra. Derivatives with different sulfurated moieties are obtained as well through thio-Michael addition of thiols on ascorbyl acrylates. The new amphiphilic structures exhibit very high antioxidant activity using the DPPH assay.

Synthesis and spectroscopic characterization of double chained and sulfurated derivatives of L-ascorbic acid / Tanini, Damiano; Gori, Marianna; Bicocchi, Francesco; Ambrosi, Moira; Pierandrea Lo Nostro, ; Capperucci, Antonella. - In: ARKIVOC. - ISSN 1551-7012. - ELETTRONICO. - part (ii):(2016), pp. 407-420. [10.24820/ark.5550190.p009.781]

Synthesis and spectroscopic characterization of double chained and sulfurated derivatives of L-ascorbic acid

TANINI, DAMIANO;AMBROSI, MOIRA;LO NOSTRO, PIERANDREA;CAPPERUCCI, ANTONELLA
2016

Abstract

Lipophilic saturated and unsaturated L-ascorbyl 5,6-O-diesters from fatty acids are prepared and fully characterized through NMR and MS spectra. Derivatives with different sulfurated moieties are obtained as well through thio-Michael addition of thiols on ascorbyl acrylates. The new amphiphilic structures exhibit very high antioxidant activity using the DPPH assay.
2016
part (ii)
407
420
Goal 3: Good health and well-being for people
Tanini, Damiano; Gori, Marianna; Bicocchi, Francesco; Ambrosi, Moira; Pierandrea Lo Nostro, ; Capperucci, Antonella
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1071741
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