Use of an allylic anchor group and of its palladium catalyzed hydrostannolytic cleavage in the solid phase synthesis of protected peptide fragments
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Selective cleavage of the allyl and (allyloxy)carbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis
2. The Allyloxycarbonyl (Aloc) Moiety?Conversion of an Unsuitable into a Valuable Amino Protecting Group for Peptide Synthesis
3. Synthesis of Glycopeptides, Partial Structures of Biological Recognition Components[New Synthetic Methods(67)]
4. Solid Phase Synthesis of Peptides and Glycopeptides on Polymeric Supports with Allylic Anchor Groups
5. Simultaneous multiple synthesis of protected peptide fragments on ‘allyl’-functionalized cellulose disc supports
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1. Resin-to-Resin Transfer Reactions (RRTR) via Sonogashira Coupling;Solid-Phase Organic Syntheses;2012-06-14
2. LINKERS FOR SOLID-PHASE SYNTHESIS;The Combinatorial Index;2012
3. Synthetic Approaches for Total Chemical Synthesis of Proteins and Protein-Like Macromolecules of Branched Architecture;Current Organic Chemistry;2006-09-01
4. Development of resin-to-resin transfer reactions (RRTR) using Sonogashira chemistry;Tetrahedron;2005-02
5. Polypeptide Synthesis, Solid-Phase Method;Encyclopedia of Polymer Science and Technology;2004-07-15
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