The condensation of 2,6-dichloroimidazo[1,2-a]pyridine with ribonolactone gives a novel imidazo[1,2-a]pyridine C-nucleoside with an unexpected site of ribosylation
- 1 April 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (14) , 2365-2368
- https://doi.org/10.1016/0040-4039(96)00292-4
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Design, Synthesis, and Antiviral Activity of Certain 2,5,6-Trihalo-1-(.beta.-D-ribofuranosyl)benzimidazolesJournal of Medicinal Chemistry, 1995
- Thiazole-Based Synthesis of Formyl C-GlycosidesThe Journal of Organic Chemistry, 1994
- Benzimidazole Ribonucleosides: Design, Synthesis, and Antiviral Activity of Certain 2-(Alkylthio)- and 2-(Benzylthio)-5,6-dichloro-1-(.beta.-D-ribofuranosyl)benzimidazolesJournal of Medicinal Chemistry, 1994
- Synthesis and cytotoxic activity of C-glycosidic nicotinamide riboside analogsJournal of Medicinal Chemistry, 1992
- A Direct Route to 3‐(D‐Ribofuranosyl)pyridine NucleosidesHelvetica Chimica Acta, 1991
- 1 The Chemistry and Biochemistry of C-Nucleosides and C-ArylglycosidesPublished by Elsevier ,1985
- 5 The Chemistry and Biochemistry of C-NucleosidesProgress in Medicinal Chemistry, 1976
- Benzimidazole nucleosides, nucleotides, and related derivativesChemical Reviews, 1970
- The synthesis of 2‐chloro‐1‐(β‐D‐ribofuranosyl)benzimidazole and certain related derivativesJournal of Heterocyclic Chemistry, 1968
- Syntheses of substituted imidazo[1,2-a]pyridines via "ylide-like" intermediatesThe Journal of Organic Chemistry, 1968