Acid-labile anchoring linkages for solid phase synthesis of C-terminal asparagine peptides using the Fmoc strategy
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1990.tb00964.x/fullpdf
Reference32 articles.
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3. SOLID-PHASE PEPTIDE SYNTHESIS OF SOMATOSTATIN USING MILD BASE CLEAVAGE OF Nα-9- FLUORENYLMETHYLOXYCARBONYLAMINO ACIDS
4. Peptide synthesis. Part 2. Procedures for solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino-acids on polyamide supports. Synthesis of substance P and of acyl carrier protein 65–74 decapeptide
5. Peptide synthesis. Part 5. Solid-phase synthesis of [15-leucine]little gastrin
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1. Diisocyanates as scaffolds for combinatorial libraries. The solid-phase synthesis of bis-ureas from polymer-supported diisocyanates;Tetrahedron Letters;1996-11
2. Combinatorial synthesis — the design of compound libraries and their application to drug discovery;Tetrahedron;1995-07
3. Design, synthesis and potential use of 3,9-substituted xanthene handles for Solid Phase Peptide Synthesis;Journal f�r Praktische Chemie/Chemiker-Zeitung;1994
4. A dilute TFA-labile resin linkage for the Fmoc solid phase synthesis of protected peptide amides;Peptides;1994
5. Studies on the acylation of hydroxy-functionalized resins using Fmoc amino acids activated using diisopropylcarbodiimide/HOBt or as acid fluorides;Tetrahedron;1993-01
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