A Tractable and Efficient One-Pot Synthesis of 5'-Azido-5'-deoxyribonucleosides
Theodore V. Peterson, Tobin U. B. Streamland, Ahmed M. Awad
Molecules · 2014
doi:10.3390/molecules19022434 (opens in a new tab)
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Abstract
Synthetic routes to 5'-azidoribonucleosides are reported for adenosine, cytidine, guanosine, and uridine, resulting in a widely applicable one-pot methodology for the synthesis of these and related compounds. The target compounds are appropriate as precursors in a variety of purposive syntheses, as the synthetic and therapeutic relevance of azido- and amino-modified nucleosides is expansive. Furthermore, in the conversion of alcohols to azides, these methods offer a tractable alternative to the Mitsunobu and other more difficult reactions.
Abstract licence: CC BY
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