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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/121944
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dc.contributor.authorSarkar, M.R.-
dc.contributor.authorDasgupta, S.-
dc.contributor.authorPyke, S.M.-
dc.contributor.authorBell, S.G.-
dc.date.issued2019-
dc.identifier.citationChemical Communications, 2019; 55(34):5029-5032-
dc.identifier.issn1359-7345-
dc.identifier.issn1364-548X-
dc.identifier.urihttp://hdl.handle.net/2440/121944-
dc.description.abstractThe cytochrome P450 monooxygenase CYP101B1 from Novosphingobium aromaticivorans selectively hydroxylated methylene C-H bonds in cycloalkyl rings. Cycloketones and cycloalkyl esters containing C6, C8, C10 and C12 rings were oxidised with high selectively on the opposite side of the ring to the carbonyl substituent. Cyclodecanone was oxidised to oxabicycloundecanol derivatives in equilibrium with the hydroxycyclodecanones.-
dc.description.statementofresponsibilityMd Raihan Sarkar, Samrat Dasgupta, Simon M. Pyke and Stephen G. Bell-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsThis journal is © The Royal Society of Chemistry 2019-
dc.source.urihttp://dx.doi.org/10.1039/c9cc02060h-
dc.subjectBiocatalytic hydroxylation-
dc.titleSelective biocatalytic hydroxylation of unactivated methylene C-H bonds in cyclic alkyl substrates-
dc.typeJournal article-
dc.identifier.doi10.1039/c9cc02060h-
pubs.publication-statusPublished-
dc.identifier.orcidPyke, S.M. [0000-0002-0061-5115]-
dc.identifier.orcidBell, S.G. [0000-0002-7457-9727]-
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Chemistry publications

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