A new protecting group for aspartic acid that minimizes piperidine-catalyzed aspartimide formation in Fmoc solid phase peptide synthesis
- 1 June 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (24), 4243-4246
- https://doi.org/10.1016/0040-4039(96)00807-6
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- N-2-hydroxy-4-methoxybenzyl (Hmb) backbone protection strategy prevents double aspartimide formation in a ‘difficult’ peptide sequenceTetrahedron Letters, 1995
- Aspartimide formation in base-driven 9-fluorenylmethoxycarbonyl chemistryTetrahedron Letters, 1994
- Piperidine-mediated side product formation for Asp(OBut)-containing peptidesJournal of the Chemical Society, Chemical Communications, 1994
- Formation of aspartimide peptides in Asp-Gly sequencesTetrahedron Letters, 1989
- Amino acids and peptides. XXV. Application of newly developed .BETA.-1- and .BETA.-2-adamantylaspartates to peptide synthesis by solid phase and conventional solution methods.CHEMICAL & PHARMACEUTICAL BULLETIN, 1989
- Amino acids and peptides. Part 19. Synthesis of β-1- and β-2-adamantyl aspartates and their evaluation for peptide synthesisJournal of the Chemical Society, Perkin Transactions 1, 1988
- Effect of piperidine on benzylaspartyl peptides in solution and in the solid phaseJournal of the Chemical Society, Chemical Communications, 1983
- SIDE REACTIONS IN PEPTIDE SYNTHESISInternational Journal of Peptide and Protein Research, 1978
- SIDE REACTIONS IN PEPTIDE SYNTHESISInternational Journal of Peptide and Protein Research, 1978
- SIDE REACTIONS IN PEPTIDE SYNTHESIS. VI.International Journal of Peptide and Protein Research, 1978