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Cobalamin-Dependent Apparent Intramolecular Methyl Transfer for Biocatalytic Constitutional Isomerization of Catechol Monomethyl Ethers
Author(s) -
Judith E. Farnberger,
Katharina Hiebler,
Sarah Bierbaumer,
W. Skibar,
Ferdinand Zepeck,
Wolfgang Kroutil
Publication year - 2019
Publication title -
acs catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.898
H-Index - 198
ISSN - 2155-5435
DOI - 10.1021/acscatal.8b05072
Subject(s) - isomerization , chemistry , catechol , moiety , cobalamin , biocatalysis , intramolecular force , ether , stereochemistry , catalysis , reaction mechanism , organic chemistry , biochemistry , vitamin b12
Isomerization is a fundamental reaction in chemistry. However, isomerization of phenyl methyl ethers has not been described yet. Using a cobalamin-dependent methyl transferase, a reversible shuttle concept was investigated for isomerization of catechol monomethyl ethers. The methyl ether of substituted catechol derivatives was successfully transferred onto the adjacent hydroxy moiety. For instance, the cobalamin-dependent biocatalyst transformed isovanillin to its regioisomer vanillin with significant regioisomeric excess (68% vanillin). To the best of our knowledge, isomerization by methyl transfer employing a methyl transferase has not been reported before.

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