
Phytochemistry p. 271 - 274 (1997)
Update date:2022-08-29
Topics:
Cohen, Peter A.
Neil Towers
Chlorination of the anthraquinones, emodin and 7-chloroemodin, was studied with an enzyme preparation from the lichen Nephroma laevigatum, and a commerically available fungal chloroperoxidase (EC 1.11.1.10). The fungal enzyme converted emodin to a mixture of 5-chloro, 7-chloro and 5,7- dichloroemodin, while converting the 7-chloro isomer to 5,7-dichloroemodin in nearly quantitative yield. The lichen enzyme, however, chlorinated emodin only at C-7 and failed to chlorinate 7-chloroemodin further. In non-enzymic controls, emodin gave the same set of products as the fungal enzyme but 7- chloroemodin did not undergo further chlorination. The chemical structures of the products were confirmed from UV, El-mass and 1H NMR spectral data.
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Doi:10.1080/00945719708000159
(1997)Doi:10.1021/acs.inorgchem.0c02408
(2020)Doi:10.1007/s10593-016-1828-4
(2016)Doi:10.1002/chem.200903418
(2010)Doi:10.1016/S0040-4020(01)00428-8
(2001)Doi:10.1002/hlca.19610440335
(1961)