Issue 5, 1983

Preparation of key intermediates for the synthesis of C-nucleosides and other derivatives of 1-deoxyribose

Abstract

The reaction of D-ribose with stabilised ylides can be made to yield solely acyclic products, which may then be cyclised with high stereoselectivity using phenylselenenyl chloride to produce 1-β-substituted 1-deoxyribose derivatives.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 224-226

Preparation of key intermediates for the synthesis of C-nucleosides and other derivatives of 1-deoxyribose

P. D. Kane and J. Mann, J. Chem. Soc., Chem. Commun., 1983, 224 DOI: 10.1039/C39830000224

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