Stepwise Solid-Phase Synthesis of Serine-, Tyrosine- and Homoserine-nucleopeptides
- 1 July 1997
- journal article
- research article
- Published by Taylor & Francis in Nucleosides and Nucleotides
- Vol. 16 (7-9) , 1487-1488
- https://doi.org/10.1080/07328319708006212
Abstract
Hydroxylated amino acids can be introduced in nucleopeptides using the acetyl group for their side chain protection. Base-stable nucleopeptide analogues are obtained if homoserine is used as the linking residue.Keywords
This publication has 6 references indexed in Scilit:
- Peptide-Oligonucleotide Hybrids with N-Acylphosphoramidate LinkagesThe Journal of Organic Chemistry, 1995
- Solid-phase synthesis of a nucleopeptide from the linking site of adenovirus-2 nucleoprotein, -Ser(p5′CATCAT)-Gly-Asp-. Convergent versus stepwise strategyNucleic Acids Research, 1995
- Stepwise Solid-Phase Synthesis of the Nucleopeptide Phac-Phe-Val-Ser(p3'ACT)-Gly-OHThe Journal of Organic Chemistry, 1994
- DNA TOPOISOMERASE POISONS AS ANTITUMOR DRUGSAnnual Review of Biochemistry, 1989
- Phages with Protein Attached to the DNA EndsPublished by Springer Nature ,1988
- Initiation of Viral DNA ReplicationPublished by Elsevier ,1988