Chiral Synthons by Enantioselective Hydrolysis of meso-Diesters with Pig Liver Esterase: Substrate-Stereoselectivity Relationships
The enantioselective synthesis of some antibiotics by combination of enzymatic and non-enzymatic procedures brought us to look at the substrate-stereoselectivity relationships in more detail. The enantiomeric excess of the chiral half-esters (Scheme 1), and even the absolute configuration of these...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | deu |
| Published: |
Swiss Chemical Society
1986-09-01
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| Series: | CHIMIA |
| Online Access: | https://www.chimia.ch/chimia/article/view/9748 |
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