PREPARATION OF FURTHER 2-PHENYLISOPROPYLOXYCARBONYL AMINO ACIDS FOR APPLICATION IN SOLID PHASE PEPTIDE SYNTHESIS
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1975.tb02472.x/fullpdf
Reference14 articles.
1. Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide
2. Acid stability of several benzylic protecting groups used in solid-phase peptide synthesis. Rearrangement of O-benzyltyrosine to 3-benzyltyrosine
3. Peptidsynthesen unter verwendung der 2-(p-diphenyl)-isopropyl-oxycarbonyl (dpoc)-aminoschutzgruppe
4. PREPARATION OF SOME 2-PHENYLISOPROPYLOXYCARBONYL AMINO ACIDS. EVALUATION OF THEIR PROPERTIES WITH PARTICULAR REFERENCE TO APPLICATION IN SOLID PHASE PEPTIDE SYNTHESIS
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1. Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids;International Journal of Peptide and Protein Research;2009-01-12
2. SOLID PHASE SYNTHESIS OF APAMIN, THE PRINCIPAL NEUROTOXIN IN BEE VENOM*;International Journal of Peptide and Protein Research;2009-01-12
3. Differential Protection and Selective Deprotection in Peptide Synthesis;Protection of Functional Groups in Peptide Synthesis;1981
4. The Composite Physical and Chemical Approach to the Solution Spatial Structure of Polypeptide Neurotoxins;Advances in Solution Chemistry;1981
5. BIOPOLYMER SYNTHESIS ON SOLID SUPPORTS;Chemistry for the Welfare of Mankind;1979
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