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- DOI: 10.1039/b617537f
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Enantioselective oxidation of O-methyl-N-hydroxylamines using monoamine oxidase N as catalyst
Eve, T S C; Wells, A; Turner, N J
Chemical Communications. 2007;(15):1530-1531.
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Full-text held externally
- DOI: 10.1039/b617537f
Abstract
Enantioselective oxidation of racemic O-methyl-N-hydroxy-cyclohexylethylamine, using a variant of monoamine oxidase N (MAO-N) from Aspergillus niger, yields unreacted (R)-enantiomer (e.e. = 99%) together with the oxime exclusively in the (E)-configuration.
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Language:
english
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Issue:
15
Start page:
1530
End page:
1531
Total:
2
Pagination:
1530-1531
Digital Object Identifier:
10.1039/b617537f
ISI Accession Number:
ISI:000245423800014
General notes:
- Eve, Tom S. C. Wells, Andrew Turner, Nicholas J. 12 ROYAL SOC CHEMISTRY CAMBRIDGE 153HU
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Active
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Manchester eScholar ID:
uk-ac-man-scw:1f701
Created:
7th September, 2009, 15:11:17
Last modified:
7th September, 2009, 15:11:17