| Weight | 86.09 g/mol |
|---|---|
| Formula | C4H6O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
beta-Butyrolactone (36536-46-6, 3068-88-0)
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- Preparation of predominantly syndiotactic poly(.beta.-hydroxybutyrate) by the tributyltin methoxide catalyzed ring-opening polymerization of racemic .beta.-butyrolactone (Macromolecules, 1993)
- Thermal properties and stereoregularity of poly(3-hydroxybutyrate) prepared from optically active .beta.-butyrolactone with a zinc-based catalyst (Macromolecules, 1991)
- Polylactones. 35. Macrocyclic and Stereoselective Polymerization of .beta.-D,L-Butyrolactone with Cyclic Dibutyltin Initiators (Macromolecules, 1995)
- Ring-opening polymerization of optically active .beta.-butyrolactone using distannoxane catalysts: synthesis of high-molecular-weight poly(3-hydroxybutyrate) (Macromolecules, 1993)
- Ring-opening copolymerization of optically active .beta.-butyrolactone with several lactones catalyzed by distannoxane complexes: synthesis of new biodegradable polyesters (Macromolecules, 1993)
- Stereoselective reactions. 14. Efficient enantioselective construction of quaternary carbon centers by the sequential dialkylation of (S)-.gamma.-[(trityloxy)methyl]-.gamma.-butyrolactone. Synthesis of optically active .beta.,.beta.-disubstituted .gamma.-butyrolactones (Journal of Organic Chemistry, 1988)
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SMILESCC1CC(=O)O1
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InChIKeyGSCLMSFRWBPUSK-UHFFFAOYSA-N
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beta-Butyrolactone
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