The nsults from the baker's yeast-mediated reduction of the acetates 3a-d and the methyl ethers 5a-d wete compared with the same biotransformation which converts the a-hydroxy ketones lad into the (R)-diols 2ad (90-989bee); the acetates 3ad afford the (S)-monoacetates 4o-d (7294% ee) and the methyl
Stereochemical Course of Baker's Yeast Mediated Reduction of the Tri- and Tetrasubstituted Double Bonds of Substituted Cinnamaldehydes
β Scribed by Giovanni Fronza; Claudio Fuganti; Stefano Serra
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 637 KB
- Volume
- 2009
- Category
- Article
- ISSN
- 1434-193X
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