Literature DB >> 18613694

2-Arylhydroxytyrosol derivatives via Suzuki-Miyaura cross-coupling.

Roberta Bernini1, Sandro Cacchi, Giancarlo Fabrizi, Eleonora Filisti.   

Abstract

2-Arylhydroxytyrosol derivatives, a new class of hydroxytyrosol derivatives, have been prepared in high to excellent yields from the corresponding 2-chloro precursors via Suzuki-Miyaura cross-coupling with arylboronic acids containing electron-donating, electron-withdrawing, as well as ortho substituents. A remarkable halide effect has been observed. 2-Iodo- and 2-bromohydroxytyrosol derivatives have been found to be ineffective cross-coupling partners in many cases. The acetonide and carbonate protecting groups can be readily removed.

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Year:  2008        PMID: 18613694     DOI: 10.1021/ol8012292

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Synthesis and Evaluation of the Antioxidant Activity of Lipophilic Phenethyl Trifluoroacetate Esters by In Vitro ABTS, DPPH and in Cell-Culture DCF Assays.

Authors:  Roberta Bernini; Maurizio Barontini; Valentina Cis; Isabella Carastro; Daniela Tofani; Rosa Anna Chiodo; Paolo Lupattelli; Sandra Incerpi
Journal:  Molecules       Date:  2018-01-19       Impact factor: 4.411

2.  Synthesis of Lipophilic Esters of Tyrosol, Homovanillyl Alcohol and Hydroxytyrosol.

Authors:  Roberta Bernini; Isabella Carastro; Francesca Santoni; Mariangela Clemente
Journal:  Antioxidants (Basel)       Date:  2019-06-14

3.  New lipophilic piceatannol derivatives exhibiting antioxidant activity prepared by aromatic hydroxylation with 2-iodoxybenzoic acid (IBX).

Authors:  Roberta Bernini; Maurizio Barontini; Carmela Spatafora
Journal:  Molecules       Date:  2009-11-17       Impact factor: 4.411

  3 in total

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