4.4 Article

Synthesis of a C3-symmetric nanoscale molecular platform based on marine cyclopeptides

Journal

SYNLETT
Volume -, Issue 6, Pages 1003-1006

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-2004-822906

Keywords

amino acids; condensation; cyclizations; heterocycles; peptides

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Efficient synthesis of a conformationally preorganized C-3-symmetric molecular platform is reported. The rigid scaffold is based on the structure of marine cyclopeptides and presents three functional groups pointing in the same direction. The bicyclic imidazole building blocks were synthesized in seven steps from trans-4-hydroxy-(S)-proline.

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