The biotransformation of (^)-bicyclo [3.3.1]nonane-2,6-dione by Aspergillus niger and Glomerella cingulata was investigated. The diketone was reduced to the ketoalcohol 2-endo-hydroxy-bicyclo[3.3.1]nonane-6-one and the diol endo,endo-bicyclo[3.3.1]nonane-2,6-diol respectively. Endo,endobicyclo[3.3.1
Screening of Yeast Species for the Stereoselective Reduction of Bicyclo[2.2.2]octane-2,6-dione.
✍ Scribed by Adriana L. Botes; Daniel Harvig; Martha S. van Dyk; Ian Sarvary; Torbjoern Frejd; Mikael Katz; Baerbel Hahn-Haegerdal; Marie F. Gorwa-Grauslund
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0931-7597
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