| Literature DB >> 3410044 |
S Kawai1, T Umezawa, M Shimada, T Higuchi.
Abstract
It was found that 2,4-di(tert-butyl)-4-(methoxycarbonylmethyl)-2-buten-4-ol ide (II) was formed as an aromatic ring cleavage product of a phenolic lignin model compound, 4,6-di(tert-butyl)guaiacol (I), by laccase of Coriolus versicolor. Based on isotopic experiments with 18O2 and H2 18O, the mechanism of formation of II from I is discussed.Entities:
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Year: 1988 PMID: 3410044 DOI: 10.1016/0014-5793(88)80043-7
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124