Solid-phase synthesis of “head-to-tail” cyclic peptides via lysine side-chain anchoring
✍ Scribed by Jordi Alsina; Francesc Rabanal; Ernest Giralt; Fernando Albericio
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 385 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Head-to-side-chain" cyclic tripeptides were designed as endothelin receptor antagonists. Solid phase synthesis of cyclic peptides, using an automated allyl cleavage procedure with Pd[P(Ph3)]a followed by cyclization was performed. Synthetic procedures were established on a continous-flow peptide syn
Conditions for the synthesis of i -(i +4) side chain-to-side chain head-to-tail Lys Glu and Glu Lys linked cyclic peptides related to hypoglycaemic analogues of human growth hormone hGH [6-13] have been examined. The success of the cyclisation reaction with the corresponding resin-bound, partially p
## Abstract Many naturally occurring peptide acids, e.g., somatostatins, conotoxins, and defensins, contain a cysteine residue at the C‐terminus. Furthermore, installation of C‐terminal cysteine onto epitopic peptide sequences as a preliminary to conjugating such structures to carrier proteins is a