Introduction of a lipophilic thioether tether in the minor groove of nucleic acids for antisense applications
- 31 December 1993
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 3 (12) , 2765-2770
- https://doi.org/10.1016/s0960-894x(01)80760-5
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- A Rapid Solid Phase Method for the Synthesis of 3′-Thiol Group Containing OligonucleotidesNucleosides and Nucleotides, 1993
- Chemical Modifications to Improve Uptake and Bioavailability of Antisense OligonucleotidesAnnals of the New York Academy of Sciences, 1992
- Novel functionalization of the sugar moiety of nucleic acids for multiple labeling in the minor grooveTetrahedron Letters, 1991
- A simple method for the introduction of thiol group at 5′-termini of oligodeoxynucleotidesNucleic Acids Research, 1989
- Synthesis of Modified Building Blocks Containing Amino or Thiol Moieties: Application of Modified OligodeoxyribonucleotidesNucleosides and Nucleotides, 1988
- The preparation and application of functionalised synthetic oligonucleotides: III. Use of H-phosphonate derivatives of protected amino-hexanol and mercapto-propanol or-hexanolNucleic Acids Research, 1988
- Introduction of 5′-terminal functional groups into synthetic oligonucleotides for selective immobilizationAnalytical Biochemistry, 1987
- The synthesis of protected 5′-mercapto-2′,5′-dideoxyribonucleoside-3′-0-phosphorainidites; uses of 5′-mercapto-oligodeoxyribonucleotidesNucleic Acids Research, 1987
- Efficient methods for attachment of thiol specific probes to the 3′-ends of synthetic oligodeoxyribonucleotidesNucleic Acids Research, 1987
- Chemical synthesis of oligonucleotides containing a free sulphydryl group and subsequent attachment of thiol specific probesNucleic Acids Research, 1985