Selective biocatalytic hydroxylation of unactivated methylene C-H bonds in cyclic alkyl substrates.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
23 Apr 2019
Historique:
pubmed: 11 4 2019
medline: 8 5 2019
entrez: 11 4 2019
Statut: ppublish

Résumé

The 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.

Identifiants

pubmed: 30968888
doi: 10.1039/c9cc02060h
doi:

Substances chimiques

Cycloparaffins 0
carbene 2465-56-7
Cytochrome P-450 Enzyme System 9035-51-2
Methane OP0UW79H66

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5029-5032

Auteurs

Md Raihan Sarkar (MR)

Department of Chemistry, University of Adelaide, Adelaide, SA 5005, Australia. stephen.bell@adelaide.edu.au.

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Classifications MeSH