A Convenient Method for C-Azanucleosides Synthesis
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (17), 6079-6082
- https://doi.org/10.1021/jo960523i
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Synthesis of C‐nucleosides via coupling of ribosyl fluoride with typical aromatic heterocycles bearing a TMS groupHeteroatom Chemistry, 1995
- Synthesis of C-Ribo-nucleosides Having Typical Aromatic Heterocycles as Base MoietyChemistry Letters, 1994
- Synthesis and biological activity of acyclic anlogues of nojirimycinJournal of the Chemical Society, Perkin Transactions 1, 1994
- Synthesis of C-nucleosides via radical coupling reactionJournal of the Chemical Society, Perkin Transactions 1, 1994
- Reactivity of carbocyclic four-membered radicals for the preparation of carbocyclic analogues of oxetanocinsJournal of the Chemical Society, Perkin Transactions 1, 1994
- Radical decarboxylative alkylation onto heteroaromatic bases with trivalent iodine compoundsJournal of the Chemical Society, Perkin Transactions 1, 1993
- A Facile Preparative Method of C-NucleosidesChemistry Letters, 1992
- Chemical stability of a prostacyclin analog due to the absence of intramolecular catalysisThe Journal of Organic Chemistry, 1988
- C-Nucleosides and related compounds. XIV. The synthesis of a nitrogen analogue of showdomycinCanadian Journal of Chemistry, 1977
- 498. The use of thiophen as a chain-extender. Part III. Synthetic amino-acidsJournal of the Chemical Society, 1962