Synthesis of an olefin-containing cyclic peptide using the solid-phase Horner–Emmons reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. Introduction of a Chemical Constraint in a Short Peptide Derived from Human Acidic Fibroblast Growth Factor Elicits Mitogenic Structural Determinants
2. C-Terminal Cyclization of an SDF-1 Small Peptide Analogue Dramatically Increases Receptor Affinity and Activation of the CXCR4 Receptor
3. Downsizing of an HIV–cell fusion inhibitor, T22 ([Tyr 5, 12 , Lys 7 ]-Polyphemusin II), with the maintenance of anti-HIV activity and solution structure 1
4. Synthesis of Biologically Active Dicarba Analogues of the Peptide Hormone Oxytocin Using Ring-Closing Metathesis
5. Olefin Metathesis in the Design and Synthesis of a Globally Constrained Grb2 SH2 Domain Inhibitor
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1. Studies on Substrate Specificity at PR/p3 Cleavage Site of HTLV-1 Protease;International Journal of Peptide Research and Therapeutics;2007-01-10
2. Cyclic, modified and conjugated peptides;Amino Acids, Peptides and Proteins;2007
3. Magnetic CLEAR Supports for Solid-Phase Synthesis of Peptides and Small Organic Molecules;International Journal of Peptide Research and Therapeutics;2006-12-08
4. Evaluations of substrate specificity and inhibition at PR/p3 cleavage site of HTLV-1 protease;Bioorganic & Medicinal Chemistry Letters;2006-07
5. Solid-Phase Syntheses of Olefin-Containing Inhibitors for HTLV-1 Protease Using the Horner−Emmons Reaction;The Journal of Organic Chemistry;2005-11-11
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