Native Chemical Ligation with Aspartic and Glutamic Acids as C‐Terminal Residues: Scope and Limitations
- 7 August 2003
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2003 (17) , 3267-3272
- https://doi.org/10.1002/ejoc.200300032
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Preparation of an aspartic acid-containing protected peptideInternational Journal of Peptide and Protein Research, 2009
- Synthesis of β and γ-fluorenylmethyl esters of respectively Nα-Boc-L-aspartic acid and Nα-Boc-L-glutamic acidInternational Journal of Peptide and Protein Research, 2009
- Synthesis of Proteins by Native Chemical LigationScience, 1994
- Development of a Linker with an Enhanced Stability for the Preparation of Peptide Thioesters and Its Application to the Synthesis of a Stable-Isotope-Labelled HU-Type DNA-Binding ProteinBulletin of the Chemical Society of Japan, 1993
- In situ neutralization in Boc‐chemistry solid phase peptide synthesisInternational Journal of Peptide and Protein Research, 1992
- Synthesis of S‐alkyl and C‐terminal analogs of the Saccharomyces cerevisiae a‐factorInternational Journal of Peptide and Protein Research, 1991
- Polypeptide Synthesis Using the S-Alkyl Thioester of a Partially Protected Peptide Segment. Synthesis of the DNA-Binding Domain of c-Myb Protein (142–193)–NH2Bulletin of the Chemical Society of Japan, 1991
- Side reactions in peptide synthesis. 8. On the phenacyl group in the protection of the .beta.-carboxyl function of aspartyl residuesThe Journal of Organic Chemistry, 1978
- Phenacyl photosensitive blocking groupsThe Journal of Organic Chemistry, 1973
- The Total Synthesis of Cephalosporin C1Journal of the American Chemical Society, 1966