Metal Mediated Reactions in Nucleside Synthesis
- 1 January 1991
- journal article
- abstracts
- Published by Taylor & Francis in Nucleosides and Nucleotides
- Vol. 10 (1-3) , 499-500
- https://doi.org/10.1080/07328319108046507
Abstract
The reaction of a halogenated nucleoside with cuprous ions and appropriate nucleophiles allows for the introduction of a wide range of functional groups or synthons into specific postions of the base molety of nucleosides.Keywords
This publication has 7 references indexed in Scilit:
- Copper mediated reactions in nucleoside synthesisTetrahedron Letters, 1990
- New methodologies for the synthesis of C-2 functionalized hypoxanthine nucleosidesThe Journal of Organic Chemistry, 1988
- Novel approaches to functionalized nucleosides via palladium-catalyzed cross coupling with organostannanesJournal of the American Chemical Society, 1987
- Palladium-catalyzed cross-coupling of 2-iodoadenosine with terminal alkynes: Synthesis and biological activities of 2-alkynyladenosines.CHEMICAL & PHARMACEUTICAL BULLETIN, 1985
- Tetrahedron report number 163Tetrahedron, 1984
- Synthesis and antiviral activity of certain 9-.beta.-D-ribofuranosylpurine-6-carboxamidesJournal of Medicinal Chemistry, 1981
- Nucleic acid related compounds. 31. Smooth and efficient palladium-copper catalyzed coupling of terminal alkynes with 5-iodouracil nucleosidesTetrahedron Letters, 1981