EventsThe 16th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 16th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Oct, 2012
Citation
Marcella Corda, Maria João Matos, Benedetta Era, Stefania Utzeri, Silvia Serra, Carmen Picciau, Giovanna Lucia Delogu, Antonella Fais, Synthesis of a Serie of 2-Phenylbenzofurans. Structures with Rigid Trans-resveratrol\'s Core and Their Tyrosinase Activity, in Proceedings of The 16th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2012, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-16-01109
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Synthesis of a Serie of 2-Phenylbenzofurans. Structures with Rigid Trans-resveratrol\'s Core and Their Tyrosinase Activity

Carmen Picciau 2
Stefania Utzeri 1
Maria João Matos 3
Marcella Corda 1
1. Dipartimento di Scienze della Vita e dell’Ambiente, Università degli Studi di Cagliari, Macrosezione Biomedica Complesso Universitario di Monserrato, S.S.554, 09042, Monserrato (Cagliari), Italy.
2. Dipartimento di Scienze della Vita e dell’Ambiente, Università degli Studi di Cagliari, Macrosezione di Scienze del Farmaco, Via Ospedale 72, 09124 Cagliari, Italy.
3. Departamento de Quımica Organica, Facultad de Farmacia, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain.
Abstract
Tyrosinases, better termed polyphenoloxidases (EC 1.14.18.1; monophenol, o-diphenol: oxygen oxidoreductase), are copper-containing monooxygenases catalyzing the o-hydroxylation of monophenols to the corresponding catechols (monophenolase activity) and the oxidation of catechols to the corresponding o-quinones (diphenolase activity).
Keywords
tyrosinase
benzofuran
resveratrol
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