Nucleosides, XL1Synthesis and Properties of lin-Naphthamidazole-Ribonucleosides
- 3 January 1984
- journal article
- research article
- Published by Taylor & Francis in Nucleosides, Nucleotides and Nucleic Acids
- Vol. 3 (5) , 549-557
- https://doi.org/10.1080/07328318408081289
Abstract
The fusion reaction between 1-trimethylsilylnaphth[2,3-d]imidazole (3) and its 2-methyl derivative (4) with 2,3,5-tri-O-benzoyl-1-bromo-D-ribofuranose (6) leads to anomeric mixtures of the corresponding 2'',3'',5''-tri-O-benzoyl-1.alpha.- and .beta.-D-ribofuranosylnaphth[2,3-d]imidazoles (7,11 and 9,13). Separation of the anomers was achieved by chromatographical means and debenzoylation yielded the corresponding nucleosides (8,12 and 10,14). Structural proofs are based on elementary analysis, UV- and 1H-NMR spectra.This publication has 12 references indexed in Scilit:
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