Synthesis of a New Chiral Peptide Analogue of DNA Using Ornithine Subunits and Solid‐phase Peptide Synthesis Methodologies
- 1 February 1996
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1996 (2) , 201-204
- https://doi.org/10.1002/jlac.199619960208
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Backbone modifications in oligonucleotides and peptide nucleic acid systemsCurrent Opinion in Structural Biology, 1995
- Structural studies of reagents for peptide bond formation: Crystal and molecular structures of HBTU and HATULetters in Peptide Science, 1994
- Synthesis of Peptide Nucleic Acid Monomers Containing the Four Natural Nucleobases: Thymine, Cytosine, Adenine, and Guanine and Their OligomerizationThe Journal of Organic Chemistry, 1994
- Structure-Activity Studies of the Binding of Modified Peptide Nucleic Acids (PNAs) to DNAJournal of the American Chemical Society, 1994
- Stereokontrollierte Synthese von OligonucleosidphosphorothioatenAngewandte Chemie, 1994
- Comparison of rigid and flexible backbones in antisense oligonucleotidesBioorganic & Medicinal Chemistry Letters, 1994
- Gene transfer and antisense nucleic acid techniquesParasitology Today, 1994
- PNA hybridizes to complementary oligonucleotides obeying the Watson–Crick hydrogen-bonding rulesNature, 1993
- Sequence-Selective Recognition of DNA by Strand Displacement with a Thymine-Substituted PolyamideScience, 1991
- Antisense oligonucleotides: a new therapeutic principleChemical Reviews, 1990