Synthesis of 2′-Deoxy-6,2′-Ethano-Cyclouridine1(Nucleosides and Nucleotides. Part 57)
- 1 July 1985
- journal article
- research article
- Published by Taylor & Francis in Nucleosides, Nucleotides and Nucleic Acids
- Vol. 4 (3), 401-409
- https://doi.org/10.1080/07328318508056171
Abstract
Synthesis of a carbon-bridged cyclouridine,2′-deoxy-6,2′-ethano-cyclouridine, was accomplished starting from a 2′-ketouridine via the 2′-deoxy-2′-iodoethyl-5-chlorouridine derivative through a radical cyclization.This publication has 4 references indexed in Scilit:
- Synthesis of 2′, 3′ -Dideoxy-6, 3′-Methano-cyclouridine and a Furanosyl To Pyranosyl Ring-isomerization In The C-cyclo-nucleoside (Nucleosides and Nucleotides. 531)Nucleosides, Nucleotides and Nucleic Acids, 1984
- Synthesis of 6,5'-cyclo-5'-deoxyuridines by radical cyclization (nucleosides and nucleotides. L).CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
- Synthesis of 2′-C-Nitromethyl Derivatives of Uridine and the Structure of a Carbon-Bridged Cyclonucleoside Derived Therefrom (Nucleosides and Nucleotides 51)Nucleosides, Nucleotides and Nucleic Acids, 1984
- Synthesis of 6,5'-Cyclo-5'-deoxyuridine: A Pyrimidine Nucleoside Fixed in anti ConformationHETEROCYCLES, 1982