Nucleoside analogs involving modifications in the carbohydrate ring: nuclear magnetic resonance spectroscopic studies

Abstract
The concomitant use of 1H nmr and 13C nmr spectroscopy as a probe of structure, stereochemistry, and conformation of several nucleoside analogs derived from 1-oxa-4-thiacyclohexane is described. The 1H nmr spectroscopic properties of an acyclic nucleoside analog derived from uridine are also described.

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