6-Vinylated guanosine as a novel cross-linking agent and its versatile synthesis from the 6-O-tosylate by Pd(0)-catalyzed cross-coupling
- 16 January 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (3) , 421-424
- https://doi.org/10.1016/0040-4039(94)02224-y
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- The Role of a Quinone Methide in the Sequence Specific Alkylation of DNAJournal of the American Chemical Society, 1994
- Antisense Oligonucleotides as Therapeutic Agents—Is the Bullet Really Magical?Science, 1993
- Sequence-specific double-strand alkylation and cleavage of DNA mediated by triple-helix formationJournal of the American Chemical Society, 1992
- Specific, high-efficiency, triple-helix-mediated cross-linking to duplex DNAJournal of the American Chemical Society, 1991
- A novel combined chemical-enzymic synthesis of crosslinked DNA using a nucleoside triphosphate analogBiochemistry, 1991
- Efficient, specific crosslinking and cleavage of DNA by stable, synthetic complementary oligodeoxynucleotidesJournal of the American Chemical Society, 1989
- Sequence-specific cleavage of DNA by N-bromoacetyldistamycin. Product and kinetic analysesJournal of the American Chemical Society, 1989
- Sequence-specific cross-linking of deoxyoligonucleotides via hybridization-triggered alkylationJournal of the American Chemical Society, 1986
- Palladium-catalyzed olefination of vinyl triflatesThe Journal of Organic Chemistry, 1985
- Synthesis of 2-substituted 6-methyl-9-.BETA.-D-ribofuranosylpurines.CHEMICAL & PHARMACEUTICAL BULLETIN, 1982