'Designer yeast': A new reagent for enantioselective Baeyer-Villiger oxidations
被引:57
作者:
Stewart, JD
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机构:
UNIV NEW BRUNSWICK,DEPT CHEM,ST JOHNS,NB E2L 4L5,CANADAUNIV NEW BRUNSWICK,DEPT CHEM,ST JOHNS,NB E2L 4L5,CANADA
Stewart, JD
[1
]
Reed, KW
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h-index: 0
机构:
UNIV NEW BRUNSWICK,DEPT CHEM,ST JOHNS,NB E2L 4L5,CANADAUNIV NEW BRUNSWICK,DEPT CHEM,ST JOHNS,NB E2L 4L5,CANADA
Reed, KW
[1
]
Kayser, MM
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h-index: 0
机构:
UNIV NEW BRUNSWICK,DEPT CHEM,ST JOHNS,NB E2L 4L5,CANADAUNIV NEW BRUNSWICK,DEPT CHEM,ST JOHNS,NB E2L 4L5,CANADA
Kayser, MM
[1
]
机构:
[1] UNIV NEW BRUNSWICK,DEPT CHEM,ST JOHNS,NB E2L 4L5,CANADA
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1996年
/
08期
关键词:
D O I:
10.1039/p19960000755
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The catalytic repertoire of baker's yeast has been expanded to include enantioselective Baeyer-Villiger oxidations. To create this catalyst, the Acinetobacter sp. cyclohexanone monooxygenase gene was inserted into a yeast expression vector and this was used to create a 'designer yeast' that performed oxidation reactions. Whole cell-mediated Baeyer-Villiger reactions were carried out on a 1.0 mmol scale and several cyclic ketones were converted in 20-30 h into the corresponding lactones in isolated yields of 60-83%. Under the reaction conditions, ketone reduction constituted only a minor side-reaction. Oxidation of prochiral 4-substituted cyclohexanones produced lactones with very high enantioselectivities.