臭氧分解
化学
羟基化
双键
烯丙基重排
苯甲醛
异构化
催化作用
基质(水族馆)
有机化学
漆酶
键裂
生物转化
光化学
药物化学
酶
地质学
海洋学
作者
Mathilde Lecourt,Giorgiana Chietera,Bernard Blerot,Sylvain Antoniotti
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-10-06
卷期号:26 (19): 6053-6053
被引量:5
标识
DOI:10.3390/molecules26196053
摘要
Laccase-based biocatalytic reactions have been tested with and without mediators and optimized in the oxidation of allylbenzene derivatives, such as methyl eugenol taken as a model substrate. The reaction primarily consisted in the hydroxylation of the propenyl side chain, either upon isomerization of the double bond or not. Two pathways were then observed; oxidation of both allylic alcohol intermediates could either lead to the corresponding α,β-unsaturated carbonyl compound, or the corresponding benzaldehyde derivative by oxidative cleavage. Such a process constitutes a green equivalent of ozonolysis or other dangerous or waste-generating oxidation reactions. The conversion rate was sensitive to the substitution patterns of the benzenic ring and subsequent electronic effects.
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