Molecular recognition of sec-alcohol enantiomers by Candida antarctica lipase B
✍ Scribed by Didier Rotticci; Fredrik Hæffner; Christian Orrenius; Torbjörn Norin; Karl Hult
- Book ID
- 114396346
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 142 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1381-1177
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Enantiomerically Enriched Bifunctional sec-Alcohols Prepared by Candida antarctica Lipase B Catalysis. Evidence of Non-Steric Interactions. -A biocatalytical resolution of racemic sec-alcohols is presented, since sec-alcohols are useful chiral building blocks in organic synthesis. The enantioselect
## Abstract __The active site of__ Candida antarctica __lipase B (CALB) hosts the catalytic triad (Ser‐His‐Asp), an oxyanion hole and a stereospecificity pocket. During catalysis, the fast‐reacting enantiomer of secondary alcohols places its medium‐sized substituent in the stereospecificity pocket