Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tet.2010.06.039
DC FieldValue
dc.titleHighly chemo- and regio-selective hydroxylations of o- and m-substituted toluenes to benzyl alcohols with Cellulosimicrobium cellulans EB-8-4
dc.contributor.authorDai, S.
dc.contributor.authorWu, J.
dc.contributor.authorWang, Z.
dc.contributor.authorChen, Y.
dc.contributor.authorLi, Z.
dc.date.accessioned2014-06-17T07:42:20Z
dc.date.available2014-06-17T07:42:20Z
dc.date.issued2010-08-21
dc.identifier.citationDai, 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
dc.identifier.issn00404020
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64022
dc.description.abstractHighly 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tet.2010.06.039
dc.sourceScopus
dc.subjectAlkyl toluenes
dc.subjectBenzyl alcohols
dc.subjectBiotransformations
dc.subjectEnzyme catalysis
dc.subjectHydroxylations
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1016/j.tet.2010.06.039
dc.description.sourcetitleTetrahedron
dc.description.volume66
dc.description.issue34
dc.description.page6919-6923
dc.description.codenTETRA
dc.identifier.isiut000280953500033
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