General synthesis of imidazole C-nucleosides from carbohydrate adducts of diaminomaleonitrile
- 1 January 1981
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 3,p. 110-112
- https://doi.org/10.1039/c39810000110
Abstract
The preparation of the imidazole C-nucleosides (14), (15), (20), and (21) from the adducts of ribose, arabinose, glucose, and mannose with diaminomaleonitrile is described.This publication has 4 references indexed in Scilit:
- PYRAZOFURIN METABOLISM, ENZYME-INHIBITION, AND RESISTANCE IN L5178Y-CELLS1979
- Nucleosides. 107. Synthesis of 5-(.beta.-D-arabinofuranosyl)isocytosine and related C-nucleosidesJournal of Medicinal Chemistry, 1978
- Ribopyranosyldiaminomaleonitrile: a key intermediate for the synthesis of nucleosidesJournal of the Chemical Society, Chemical Communications, 1978
- Formation of N-(2-Amino-l,2-dicyano-ethylenyl)-β-d-glucopyranosylamine in the Acidic Culture Medium Containing Diaminomaleonitrile andd-GlucoseAgricultural and Biological Chemistry, 1976