## Abstract The configurations of 1,4:3,6‐dianhydro‐2,5‐di‐__O__‐mesyl‐D‐mannitol, 1,4:3,6‐dianhydro‐2,5‐di‐__O__‐mesyl‐D‐glucitol, 1,4:3,6‐dianhydro‐2,5‐di‐__O__‐mesyl‐L‐iditol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐__O__‐mesyl‐D‐mannitol, 1,4:3:6‐dianhtydro‐2‐deoxy‐2‐iodo‐5‐__O__‐mesyl‐D‐glucitol,
Determination of the relative configuration of the C-19 to C-29 fragment of amycin B by 1H and 13C NMR investigations
✍ Scribed by Frank Hoyer; Gerhard Habermehl; Helmut Duddeck; Gábor Tóth
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 77 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
The relative configuration of a methylated undecanehexaol, a fragment of amycin B, with five chirality centers was determined by a complete 1 H and 13 C signal assignment and interpretation of its acetonide derivatives.
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