IRIS publication 57685685
Efficient kinetic bioresolution of 2-nitrocyclohexanol
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TY - JOUR - Milner, Sinead E; Brossat, Maude; Moody, Thomas S; Elcoate, Curtis J; Lawrence, Simon E; Maguire, Anita R - 2010 - Unknown - Tetrahedron: Asymmetry - Efficient kinetic bioresolution of 2-nitrocyclohexanol - Validated - () - 21 - 88 - 1011 - 1016 - The kinetic bioresoln. of 2-nitrocyclohexanol was investigated by screening a range of hydrolases both for enantioselective transesterification and for enantioselective hydrolysis of the corresponding acetate. By appropriate choice of biocatalyst and conditions, both enantiomers of cis and trans 2-nitrocyclohexanol 1 can be accessed in enantiopure form. - 0957-4166 DA - 2010/NaN ER -
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@article{V57685685, = {Milner, Sinead E and Brossat, Maude and Moody, Thomas S and Elcoate, Curtis J and Lawrence, Simon E and Maguire, Anita R}, = {2010}, = {Unknown}, = {Tetrahedron: Asymmetry}, = {Efficient kinetic bioresolution of 2-nitrocyclohexanol}, = {Validated}, = {()}, = {21}, = {88}, pages = {1011--1016}, = {{The kinetic bioresoln. of 2-nitrocyclohexanol was investigated by screening a range of hydrolases both for enantioselective transesterification and for enantioselective hydrolysis of the corresponding acetate. By appropriate choice of biocatalyst and conditions, both enantiomers of cis and trans 2-nitrocyclohexanol 1 can be accessed in enantiopure form.}}, issn = {0957-4166}, source = {IRIS} }
Data as stored in IRIS
AUTHORS | Milner, Sinead E; Brossat, Maude; Moody, Thomas S; Elcoate, Curtis J; Lawrence, Simon E; Maguire, Anita R | ||
YEAR | 2010 | ||
MONTH | Unknown | ||
JOURNAL_CODE | Tetrahedron: Asymmetry | ||
TITLE | Efficient kinetic bioresolution of 2-nitrocyclohexanol | ||
STATUS | Validated | ||
TIMES_CITED | () | ||
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VOLUME | 21 | ||
ISSUE | 88 | ||
START_PAGE | 1011 | ||
END_PAGE | 1016 | ||
ABSTRACT | The kinetic bioresoln. of 2-nitrocyclohexanol was investigated by screening a range of hydrolases both for enantioselective transesterification and for enantioselective hydrolysis of the corresponding acetate. By appropriate choice of biocatalyst and conditions, both enantiomers of cis and trans 2-nitrocyclohexanol 1 can be accessed in enantiopure form. | ||
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ISBN_ISSN | 0957-4166 | ||
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