| Weight | 130.143 g/mol |
|---|---|
| Formula | C6H10O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
PANTOLACTONE (79-50-5)
pantoyl lactone · 2,4-dihydroxy-3,3-dimethylbutyric acid gamma-lactone · pantolactone, 2-(14)C-labeled cpd, (+,-)-isomer
Score:
#4390 in Biology
,
#5548 in Chemistry
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- Diastereoface-discriminative metal coordination in asymmetric synthesis: D-pantolactone as practical chiral auxiliary for Lewis acid catalyzed Diels-Alder reactions (Tetrahedron Letters, 1985)
- d-Pantolactone as a circular dichromism (CD) calibration (Analytical Biochemistry, 1975)
- Reaction of (R)-pantolactone esters of alpha-bromoacids with amines a remarkable synthesis of optically active alpha-amino esters (Tetrahedron Letters, 1993)
- Preparation of new chiral pyrrolidinebisphosphines as highly effective ligands for catalytic asymmetric synthesis of R-()-pantolactone (Tetrahedron Letters, 1986)
- Optical resolution of racemic pantolactone with a novel fungal enzyme, lactonohydrolase. (Applied Microbiology and Biotechnology, 1995)
- Convenient access to two enantiomeric oxirane synthons bearing a quaternary gem-dimethyl carbon center: Synthesis of 3S-(+) and 3R-()-2,2-dimethyl-3,4-oxo-1-butanol from R-()-pantolactone (Tetrahedron Letters, 1986)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - pantoyl lactone
- 2,4-dihydroxy-3,3-dimethylbutyric acid gamma-lactone
- pantolactone, 2-(14)C-labeled cpd, (+,-)-isomer
- pantolactone, (R)-isomer
- pantolactone, (S)-isomer
-
SMILESCC1(COC(=O)C1O)C
-
InChIKeySERHXTVXHNVDKA-UHFFFAOYSA-N
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PANTOLACTONE
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