The γ-methyl-E-olefin as isosteric replacement of the peptide bond
- 29 January 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (5) , 703-706
- https://doi.org/10.1016/0040-4039(95)02247-3
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- The ethylene group as a peptide bond mimicking unit: A theoretical conformational analysisJournal of Computational Chemistry, 1993
- Fluoroolefin dipeptide isosteres -II. : Enantioselectlve synthesis of both antipodes of the phe-gly dlpeptide mimicTetrahedron Letters, 1990
- Fluoroolefin dipeptide isosteres — I.Tetrahedron Letters, 1990
- A stereocontrolled synthesis of trans-alkene isosteres of dipeptidesTetrahedron Letters, 1986
- A method for the determination of the configuration of the L-pro-L,D-phe pseudodipeptide isomers containing a trans-ethylene isosteric replacement of the peptide bondTetrahedron, 1986
- A theoretical and crystallographic study of the geometries and conformations of fluoro-olefins as peptide analoguesTetrahedron, 1986
- On the double bond isostere of the peptide bond: preparation of modified di- and tri-peptides incorporating proline and alanine analoguesJournal of the Chemical Society, Perkin Transactions 1, 1984
- Theoretical conformational analysis of acetyl‐alanine—methylamide double bond and methyl‐substituted doublebond isosteres of the peptide bondFEBS Letters, 1982
- On the double bond isostere of the peptide bond: preparation of an enkephalin analogueJournal of the Chemical Society, Perkin Transactions 1, 1982
- Incorporation of trans-olefinic dipeptide isosteres into enkephalin and substance P analoguesJournal of the Chemical Society, Chemical Communications, 1980