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Laccase-Catalyzed 1,4-Dioxane-Mediated Synthesis of Belladine N-Oxides with Anti-Influenza A Virus Activity.


ABSTRACT: Belladine N-oxides active against influenza A virus have been synthetized by a novel laccase-catalyzed 1,4-dioxane-mediated oxidation of aromatic and side-chain modified belladine derivatives. Electron paramagnetic resonance (EPR) analysis confirmed the role of 1,4-dioxane as a co-oxidant. The reaction was chemo-selective, showing a high functional-group compatibility. The novel belladine N-oxides were active against influenza A virus, involving the early stage of the virus replication life cycle.

SUBMITTER: Zippilli C 

PROVIDER: S-EPMC7866262 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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Laccase-Catalyzed 1,4-Dioxane-Mediated Synthesis of Belladine <i>N</i>-Oxides with Anti-Influenza A Virus Activity.

Zippilli Claudio C   Botta Lorenzo L   Bizzarri Bruno Mattia BM   Nencioni Lucia L   De Angelis Marta M   Protto Virginia V   Giorgi Gianluca G   Baratto Maria Camilla MC   Pogni Rebecca R   Saladino Raffaele R  

International journal of molecular sciences 20210129 3


Belladine <i>N</i>-oxides active against influenza A virus have been synthetized by a novel laccase-catalyzed 1,4-dioxane-mediated oxidation of aromatic and side-chain modified belladine derivatives. Electron paramagnetic resonance (EPR) analysis confirmed the role of 1,4-dioxane as a co-oxidant. The reaction was chemo-selective, showing a high functional-group compatibility. The novel belladine <i>N</i>-oxides were active against influenza A virus, involving the early stage of the virus replica  ...[more]

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