| Weight | 103.097 g/mol |
|---|---|
| Formula | C4H7O3- |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
4-Hydroxybutanoate
52352-27-9, 1320-61-2, 591-81-1
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- Synthesis of optically pure ethyl (S)-4-chloro-3-hydroxybutanoate by Escherichia coli transformant cells coexpressing the carbonyl reductase and glucose dehydrogenase genes (Applied Microbiology and Biotechnology, 2001)
- Asymmetric synthesis of (1R,3R,4R)-4-acetoxy-3-(1-((tert-butyldimethylsilyl)oxy)ethyl)-2- azetidinone and other 3-(1-Hydroxyethyl)-2-azetidinones from (S)-(+)-Ethyl 3-hydroxybutanoate: Formal total synthesis of (+)-thienamycin (Journal of the American Chemical Society, 1987)
- Preparation by yeast reduction and determination of the sense of chirality of enantiomerically pure ethyl ()-4,4,4-trichloro-3-hydroxy- and (+)-4,4,4-trifluoro-3-hydroxybutanoate (Helvetica Chimica Acta, 1984)
- Enzymatic production of ethyl (R )-4-chloro-3-hydroxybutanoate: asymmetric reduction of ethyl 4-chloro-3-oxobutanoate by an Escherichia coli transformant expressing the aldehyde reductase gene from yeast (Applied Microbiology and Biotechnology, 1997)
- Synthesis of optically active ethyl 4-chloro-3-hydroxybutanoate by microbial reduction (Applied Microbiology and Biotechnology, 1999)
- Synthesis of Ethyl (R)-4-Chloro-3-hydroxybutanoate with Recombinant Escherichia coli Cells Expressing (S)-Specific Secondary Alcohol Dehydrogenase (Bioscience, Biotechnology, and Biochemistry, 2002)
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