Minor Enantiomer Recycling: Metal Catalyst, Organocatalyst and Biocatalyst Working in Concert
Abstract A minor enantiomer recycling one‐pot procedure employing two reinforcing chiral catalysts has been developed. Continuous regeneration of the achiral starting material is effected via selective enzyme‐catalyzed hydrolysis of the minor product enantiomer from Lewis acid–Lewis base catalyzed a...
| Published in: | Chemistry – A European Journal |
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| Main Authors: | , , , , |
| Format: | Article in Journal/Newspaper |
| Language: | English |
| Published: |
Wiley
2009
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| Subjects: | |
| Online Access: | http://dx.doi.org/10.1002/chem.200901338 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchem.200901338 https://onlinelibrary.wiley.com/doi/full/10.1002/chem.200901338 |
| Summary: | Abstract A minor enantiomer recycling one‐pot procedure employing two reinforcing chiral catalysts has been developed. Continuous regeneration of the achiral starting material is effected via selective enzyme‐catalyzed hydrolysis of the minor product enantiomer from Lewis acid–Lewis base catalyzed addition of acyl cyanides to prochiral aldehydes in a two‐phase solvent system. The process provides O‐acylated cyanohydrins in close to perfect enantioselectivities, higher than those obtained in the direct process, and in high yields. A combination of a ( S , S )‐salen Ti Lewis acid and Candida antarctica lipase B provides the products with R absolute configuration, whereas the opposite enantiomer is obtained from the ( R , R )‐salen Ti complex and Candida rugosa lipase. |
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