The efficient synthesis of an octameric furanose carbopeptoid, readily purified by chromatography in ethyl acetate:hexane (2:1), is reported. Extensive NMR studies suggest that two tetrameric 5aminomethyltetrahydrofuran-2-carboxylates are prone to adopt solution conformations reminiscent of a repeat
Absence of secondary structure in a carbopeptoid tetramer of a trans-5-aminomethyl-tetrahydrofuran-2-carboxylate
✍ Scribed by Martin D. Smith; Daniel D. Long; Angeles Martín; Daniel G. Marquess; Timothy D.W. Claridge; George W.J. Fleet
- Book ID
- 104260907
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 263 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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