## Abstract Cyclic ketone 12, prepared from racemic 3‐__O__‐benzyl‐1,2:4,5‐di‐__O__‐cyclohexylidene‐__myo__‐inositol (4), was converted into the tertiary alcohols 13 and 20 by treatment with methyl‐magnesium bromide and (benzyloxymethyl)lithium, respectively. Deoxygenation, followed by hydrogenolys
✦ LIBER ✦
Synthesis of protected (±)-α- and β-carba-psicofuranose
✍ Scribed by Michael Bodenteich; Victor E. Marquez
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 669 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
Protected racemic a-and &psicofuranose were synthesized fmm a non-carbohydrate precursor which is available in both enantiomeric forms.
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