Fmoc Solid Phase Peptide Synthesis: A Practical

Fmoc Solid Phase Peptide Synthesis: A Practical Approach Peter D. White, W. C. Chan
Publisher: Oxford University Press, USA

Side-chain protecting groups employed for peptide synthesis were as .. [0168] (28) Atherton, E.; Sheppard, R. In the years since the publication of Atherton and Sheppard's volume, the technique of Fmoc solid-phase peptide synthesis has matured considerably and is now the standard approach for the routine production of peptides. Fmoc Solid Phase Peptide Synthesis: A Practical Approach; Oxford University Press: New York, 2004. Wiley: Enantioselective Synthesis of Beta-Amino Acids, 2nd Edition Enantioselective Synthesis of Beta-Amino Acids,. Solid phase peptide synthesis--a practical approach; IRL Press: Oxford, England, 1989; pp 203 [0169] (29) Gausepohl, H.; Kral, M.; Boulin, C.; Frank R. After Fmoc solid phase peptide synthesis, on-bead formylation and HPLC purification, more than 30 mg of the fully 13C/15N-labelled tripeptide 1 could be isolated in a typical batch. Doi:10.1016/S0040-4039(01)01102-9. This peptide can be easily crystallised and is therefore well .. Rink amide resin, 9-fluorenylmethoxycarbonyl (Fmoc) protected amino acid derivatives, and all the reagents for solid-phase peptide synthesis were purchased from Novabiochem (Laufelfingen, Switzerland). Fmoc Solid Phase Peptide Synthesis: A Practical Approach - Google. Return to citation in text: [1] [2]; Chan, W.