Synthesis of L-Cladinose Using Enantioselective Desymmetrization
L-Cladinose, a neutral sugar found in erythromycins and azithromycins, has been synthesized efficiently using enantioselective monobenzoylation of 2-propenylglycerol in the presence of the imine-CuCl(2) catalysts to elaborate the stereogenic quaternary center.
- Publisher
- GEORG THIEME VERLAG KG
- Issue Date
- 2008-10
- Language
- English
- Article Type
- Article
- Keywords
ASYMMETRIC TOTAL SYNTHESIS; ETUDE DES PRODUITS; MACROLIDE ANTIBIOTICS; KEDARCIDIN CHROMOPHORE; L-MYCAROSE; ERYTHROMYCIN; SPIRAMYCINE; DEGRADATION; LEUCOMYCIN; CARACTERISATION
- Citation
SYNLETT, no.16, pp.2526 - 2528
- ISSN
- 0936-5214
- Appears in Collection
- CH-Journal Papers(저널논문)
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