Selective laccase-catalyzed dimerization of phenolic compounds derived from lignin: Towards original symmetrical bio-based (bis) aromatic monomers
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A selective enzymatic process of vanillin dimerization is described.

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The divanillin is easily recovered as a precipitate.

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The selective formation of dimers by Csingle bondclass="glyphImg imgLazyJSB">C coupling was extended to six ortho-methoxy-para-substituted phenols.

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