## Abstract Efficient syntheses of rigid __C__~3~‐symmetric scaffolds based on adamantane are described. The scaffolds are available in multigram quantities and have been designed for conjugation to various natural products such as carbohydrates and peptides. They are thus valuable for the construc
Symmetrically-substituted decalin-based scaffolds
✍ Scribed by Zoi F Plyta; Eberhard Heller; Françoise Dumas; Christine Miet; Jacqueline Mahuteau; Jean d'Angelo *; Juan Caturla; Marie-Elise Tran Huu Dau
- Book ID
- 104210155
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 148 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The synthesis of a chiral scaffold was achieved by coupling a decalintriol platform with a NH-Boc protected α-ethylenic γ-amino acid. The two side chains of this molecule strongly self-associate through intramolecular hydrogen bonding involving the NH-Boc residues.
📜 SIMILAR VOLUMES
A series of eight potential peptidominu~ics has been synthesised based on the use of gluco-and allocarbohydrate derivatives as scaffolds to support appropriate side-chains which mimic the D-and Laminoacid residues of the cyclic peptide endothelin antagonist BQ123.