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https://doi.org/10.1016/j.tet.2010.06.039
Title: | Highly chemo- and regio-selective hydroxylations of o- and m-substituted toluenes to benzyl alcohols with Cellulosimicrobium cellulans EB-8-4 | Authors: | Dai, S. Wu, J. Wang, Z. Chen, Y. Li, Z. |
Keywords: | Alkyl toluenes Benzyl alcohols Biotransformations Enzyme catalysis Hydroxylations |
Issue Date: | 21-Aug-2010 | Citation: | Dai, S., Wu, J., Wang, Z., Chen, Y., Li, Z. (2010-08-21). Highly chemo- and regio-selective hydroxylations of o- and m-substituted toluenes to benzyl alcohols with Cellulosimicrobium cellulans EB-8-4. Tetrahedron 66 (34) : 6919-6923. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tet.2010.06.039 | Abstract: | Highly chemo- and regio-selective benzylic hydroxylations of o- and m-substituted toluenes were achieved with the easily available and easy-to-handle resting cells of Cellulosimicrobium cellulans EB-8-4 as biocatalysts, giving the corresponding benzyl alcohols as single product. Benzyl alcohols were obtained in 78-94% yield, demonstrating the first green, clean, and simple method for the preparation of benzyl alcohols via hydroxylations. Biotransformation of 4-methylbenzyl chloride with the same strain gave 4-methylbenzyl alcohol in 67-81% yield, suggesting a novel dehalogenation activity of the cells and providing a novel, green, and efficient method for the preparation of 4-methylbenzyl alcohol as well as the application potential in biodegradation of chlorine-containing aromatics. © 2010 Elsevier Ltd. All rights reserved. | Source Title: | Tetrahedron | URI: | http://scholarbank.nus.edu.sg/handle/10635/64022 | ISSN: | 00404020 | DOI: | 10.1016/j.tet.2010.06.039 |
Appears in Collections: | Staff Publications |
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