SNAr Cyclizations To Form Cyclic Peptidomimetics of β-Turns
- 1 October 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (41) , 10768-10769
- https://doi.org/10.1021/ja981589t
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Stereoisomeric Peptide Libraries and Peptidomimetics for Designing Selective Inhibitors of the αvβ3 Integrin for a New Cancer TherapyAngewandte Chemie International Edition in English, 1997
- Synthesis and evaluation of a library of peptidomimetics based upon the β-turnTetrahedron, 1997
- Rapid and efficient solid phase syntheses of cyclic peptides with endocyclic biaryl ether bondsTetrahedron Letters, 1997
- A systematic approach to the solid‐phase synthesis of linear and cyclic pseudopeptide libraries containing ψ[CH2NH] amide bond surrogatesChemical Biology & Drug Design, 1997
- Expedient solid-phase synthesis of putative β-turn mimetics incorporating the i + 1, i + 2, and i + 3 sidechainsTetrahedron Letters, 1996
- An approach to cyclic peptide libraries: Reducing epimerization in medium sized rings during solid phase synthesisTetrahedron Letters, 1996
- Simultaneous Solid-Phase Synthesis of .beta.-Turn Mimetics Incorporating Side-Chain FunctionalityJournal of the American Chemical Society, 1994
- Peptide Secondary Structure Mimetics: Recent Advances and Future ChallengesSynlett, 1993
- Retro‐Inverso Amide Bonds between Trifunctional Amino AcidsAngewandte Chemie International Edition in English, 1992
- Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin.Tetrahedron Letters, 1987