The synthesis of oligomers of oxetane-based dipeptide isosteres derived from L-rhamnose or D-xylose
✍ Scribed by Stephen W. Johnson; Sarah F. Jenkinson (née Barker); Donald Angus; Ignacio Pérez-Victoria; Timothy D. W. Claridge; George W. J. Fleet; Dr John H. Jones
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 252 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1075-2617
- DOI
- 10.1002/psc.622
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📜 SIMILAR VOLUMES
Conformational investigations have been undertaken on oligomers (dimers, tetramers, hexamers) of five closely related oxetane-based dipeptide isosteres. All the oligomers were subjected to a range of studies by NMR, FT-IR and CD spectroscopy. The oligomers derived from methyl 2,4-anhydro-5-azido-3-O
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