Synthesis and hybridization studies of urea and carbamate linked thymidine dimers incorporated into oligodeoxynucleosides
- 10 February 1994
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 4 (3) , 435-438
- https://doi.org/10.1016/0960-894x(94)80011-1
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Oligonucleosides: synthesis of a novel methylhydroxylamine-linked nucleoside dimer and its incorporation into antisense sequencesJournal of the American Chemical Society, 1992
- Synthesis of thymidine dimers containing internucleoside sulfonate and sulfonamide linkagesThe Journal of Organic Chemistry, 1992
- Therapeutic Applications of OligonucleotidesAnnual Review of Pharmacology and Toxicology, 1992
- Deoxyoligonucleotides bearing neutral analogs of phosphodiester linkages recognize duplex DNA via triple-helix formationJournal of the American Chemical Society, 1991
- Building blocks for oligonucleotide analogs with dimethylene sulfide, sulfoxide, and sulfone groups replacing phosphodiester linkagesThe Journal of Organic Chemistry, 1991
- Synthesis of nucleoside sulfonates and sulfonesTetrahedron Letters, 1991
- An efficient approach to the synthesis of thymidine derivatives containing phosphate-isosteric methylene acetal linkagesTetrahedron, 1991
- Boron-containing nucleic acids. 2. Synthesis of oligodeoxynucleoside boranophosphatesJournal of the American Chemical Society, 1990
- Antisense oligonucleotides: a new therapeutic principleChemical Reviews, 1990
- Synthesis of [3t̄'(O)→-5t̄'(c)]-oxyacetamido linked nucleosidesTetrahedron, 1990