Jump to main content
Jump to site search

Issue 9, 2012
Previous Article Next Article

Laccase-catalyzed oxidative phenolic coupling of vanillidene derivatives

Author affiliations

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.

Graphical abstract: Laccase-catalyzed oxidative phenolic coupling of vanillidene derivatives

Back to tab navigation

Supplementary files

Publication details

The article was received on 31 May 2012, accepted on 26 Jun 2012 and first published on 27 Jun 2012


Article type: Communication
DOI: 10.1039/C2GC35848D
Citation: Green Chem., 2012,14, 2375-2379
  •   Request permissions

    Laccase-catalyzed oxidative phenolic coupling of vanillidene derivatives

    M. Constantin, J. Conrad and U. Beifuss, Green Chem., 2012, 14, 2375
    DOI: 10.1039/C2GC35848D

Search articles by author

Spotlight

Advertisements