Data di Pubblicazione:
2021
Abstract:
: Laccases are multicopper oxidases, which have been widely investigated in recent decades
thanks to their ability to oxidize organic substrates to the corresponding radicals while producing
water at the expense of molecular oxygen. Besides their successful (bio)technological applications,
for example, in textile, petrochemical, and detoxifications/bioremediations industrial processes,
their synthetic potentialities for the mild and green preparation or selective modification of fine
chemicals are of outstanding value in biocatalyzed organic synthesis. Accordingly, this review is
focused on reporting and rationalizing some of the most recent and interesting synthetic exploitations
of laccases. Applications of the so-called laccase-mediator system (LMS) for alcohol oxidation
are discussed with a focus on carbohydrate chemistry and natural products modification as well
as on bio- and chemo-integrated processes. The laccase-catalyzed Csp2
-H bonds activation via
monoelectronic oxidation is also discussed by reporting examples of enzymatic C-C and C-O radical
homo- and hetero-couplings, as well as of aromatic nucleophilic substitutions of hydroquinones or
quinoids. Finally, the laccase-initiated domino/cascade synthesis of valuable aromatic (hetero)cycles,
elegant strategies widely documented in the literature across more than three decades, is also
presented
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
: laccase; biocatalysis; oxidation; stereoselectivity; laccase-mediator systems; Csp2 -H bonds activation; radical C-O and C-C couplings; cycloadditions
Elenco autori:
Monti, Daniela; Riva, Sergio; Ferrandi, ERICA ELISA; Bassanini, Ivan
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