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Solid-Supported Synthesis of a Peptide β-Turn Mimetic

✍ Scribed by Golebiowski, Adam; Klopfenstein, Sean R.; Shao, Xia; Chen, Jack J.; Colson, Anny-Odile; Grieb, Arthur L.; Russell, Anne F.


Book ID
120056462
Publisher
American Chemical Society
Year
2000
Tongue
English
Weight
63 KB
Volume
2
Category
Article
ISSN
1523-7060

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📜 SIMILAR VOLUMES


Methodology for the synthesis of mimetic
✍ Michael Kahn; Barbara Chen 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 183 KB

This letter describes a scenario which provides for the stereospecific intro uction of both the amino and carboxyl termini portion of a designed B-turn mimetic. Peptides and proteins are ubiquitously distributed in nature, and play critical roles in the regulation of virtually all biological process

The design and synthesis of mimetics of
✍ Michael Kahn; Susanne Wilke; Barbara Chen; Kagari Fujita; Yu-Hwei Lee; Michael E 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 410 KB

The synthesis of an 11 membered ring bis-lactam, a system which is designed as a conformationally restricted mimetic of type I and type II beta-turns is described. Computer assisted molecular modeling was used to compare the predicted low energy conformers of the turn mimetic with idealized type I a

Solid-phase synthesis of a type II′ β-tu
✍ John H Grimes Jr.; Yvonne M Angell; Wayne D Kohn 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 116 KB

The solid-phase synthesis of a dipeptide derived 2-amino-3-oxohexahydroindolizino[8,7-b]indole-5-carboxylate system (IBTM) is described. The IBTM moiety is formed via a solid-phase mediated Pictet-Spengler reaction of N-terminal tryptophan and the 4-{N-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-me