A synthesis of enantiopure methyl d-erythro-2,3-dihydroxybutanoate has been realized using two simple and consecutive reactions on d-erythronolactone as the starting material. The two reactions are lactone ring opening with hydrobromic acid in methanol and subsequent reductive debromination.
โฆ LIBER โฆ
L-erythro-2,3-Dihydroxybutanoic Acid and Related Compounds.
โ Scribed by Walsh, Patricia; Hayashi, J. A.
- Book ID
- 126815643
- Publisher
- American Chemical Society
- Year
- 1965
- Tongue
- English
- Weight
- 102 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0021-9568
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