A solid phase approach to oligomers of carbohydrate amino-acids: Secondary structure in a trimeric furanose carbopeptoid
The synthesis of oligomers of a C-arabinofuranosyl carbohydrate amino acid on a polystyrene support functionalised with a Rink linker is reported. Cleavage from the solid support gives ready access to dimeric and trimeric carbopeptides bearing a C-terminal carboxamide. Investigations into the soluti...
| Päätekijät: | , , , , |
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| Aineistotyyppi: | Journal article |
| Kieli: | English |
| Julkaistu: |
1998
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| Yhteenveto: | The synthesis of oligomers of a C-arabinofuranosyl carbohydrate amino acid on a polystyrene support functionalised with a Rink linker is reported. Cleavage from the solid support gives ready access to dimeric and trimeric carbopeptides bearing a C-terminal carboxamide. Investigations into the solution structure of these novel carbopeptoids utilising 1H NMR indicate that they adopt well defined conformations based around a repeating β-turn like structure stabilised by (i, i-2) inter-residue hydrogen bonds. |
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