Selective aliphatic carbon–hydrogen bond activation of protected alcohol substrates by cytochrome P450 enzymes
Author:
Affiliation:
1. School of Chemistry and Physics
2. University of Adelaide
3. , Australia
4. Department of Chemistry
5. University of Oxford
6. Inorganic Chemistry Laboratory
7. Oxford, UK
Abstract
Protected cyclohexanol and cyclohex-2-enol substrates were efficiently and selectively oxidised by different P450cam mutants providing a general methodology for generating substituted diols using biocatalysts.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/OB/C3OB42417K
Reference66 articles.
1. Cytochrome P450: Structure, Mechanism, and Biochemistry , ed. P. R. Ortiz de Montellano , Kluwer Academic/Plenum Publishers , New York , 3rd edn, 2005
2. A. Sigel , H.Sigel and R.Sigel , The Ubiquitous Roles of Cytochrome P450 Proteins , John Wiley & Sons , 1st edn, 2007 , vol. 3
3. Common and Uncommon Cytochrome P450 Reactions Related to Metabolism and Chemical Toxicity
4. Complex reactions catalyzed by cytochrome P450 enzymes
5. S. G. Bell , N.Hoskins , C. J. C.Whitehouse and L. L.Wong , Design and Engineering of Cytochrome P450 Systems , John Wiley & Sons , 1st edn, 2007 , vol. 3 , ch. 14, pp. 437–476
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