Synthesis of the nucleopeptides H-Phe-Tyr(pGC)-NH2and H-Phe-Ser(pGC)-Ala-OH via a phosphotriester approach
Open Access
- 1 January 1989
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 17 (8) , 2897-2905
- https://doi.org/10.1093/nar/17.8.2897
Abstract
Use of the protecting groups di-n-butylaminomethylene,2-nitrophenylsulfenyl and the ester of 2-(hydroxymethyl)-9,10-anthraquinone, enabled us for the first time to prepare nucleopeptide fragments containing 2'-deoxyguanosine and a free carboxylic acid group.This publication has 9 references indexed in Scilit:
- A convenient approach toward the preparation of nucleopeptidesTetrahedron, 1988
- Alteration of the ATG start codon of the A* protein of bacteriophage ϕX174 into an ATT codon yields a viable phage indicating that A* protein is not essential for ϕX174 reproductionFEBS Letters, 1987
- A model study directed towards the preparation of nucleopeptidesviaH-phosphonate intermediatesNucleic Acids Research, 1987
- Nucleotide chemistry. 16. Amidine protecting groups for oligonucleotide synthesisJournal of the American Chemical Society, 1986
- The bond in the bacteriophage øX174 gene A protein‐DNA complex is a tyrosyl‐5'‐phosphate esterFEBS Letters, 1984
- N‐Levulination of GuanosineHelvetica Chimica Acta, 1983
- Dialkylformamldines: depurination resistant N6-protecting group for deoxyadenosineNucleic Acids Research, 1983
- The 2-Nitrophenylsulfenyl (Nps) Group for the Protection of Amino Functions of Cytidine, Adenosine, Guanosine and Their 2'-Deoxysugar Derivatives.Acta Chemica Scandinavica, 1983
- Protein p3 is linked to the DNA of phage phi 29 through a phosphoester bond between serine and 5'-dAMP.Proceedings of the National Academy of Sciences, 1980