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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

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Conformational studies of oligomeric oxe
✍ Stephen W. Johnson; Sarah F. Jenkinson (née Barker); Ignacio Pérez-Victoria; Ali 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 197 KB

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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