## Abstract The 4‐thio analog of 2,6‐dideoxy‐D‐__ribo__‐hexopyranose (D‐digitoxose) is part of the saccharide chain of the calicheamicins and esperamicins. A straightforward synthesis of the 4‐thiodigitoxoside 12 as its diacetate 13 starting from methyl α‐D‐galactopyranoside (1) is described. Prope
✦ LIBER ✦
A stereochemically general synthesis of methyl 2,4,6-trideoxy-4-methylthio-α-D-ribo-pyranoside, the thio sugar of esperamicin A1
✍ Scribed by William R. Roush; Darin Gustin
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 417 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Actor.
A sleazy general synthesis of methyl 2,4,~~xyJI_a-~~~p~oside (lb), the thio sugar isolated from esperamicin, is described. 'I%e synthesis involves the neighbori& group assisted
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These compounds have a 4a-methyl group Jn the lactone rJng. For R3, R4 and R5 substltuents, Jn compounds & and i, see references 3 and 4.