Laccase-catalyzed oxidative phenolic coupling of vanillidene derivatives

Publication Type
Journal contribution (peer reviewed)
Authors
Constantin, M.-A.; Conrad, J.; Beifuss, U.
Year of publication
2012
Published in
Green Chem.
Band/Volume
14/
DOI
10.1039/c2gc35848d
Page (from - to)
2375 – 2379
Abstract

The laccase-catalyzed oxidative phenolic coupling of vanillidene derivatives using aerial oxygen as the oxidant has been developed. Depending on the substitution pattern of the vanillidene double bond of the substrate, either dilactones, dihydrobenzo[b]furans or biphenyls are formed.

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