Issue 21, 1994

Photocatalysed addition of alcohols to 5-substituted 2,5-dihydrofuran-2-ones: novel synthesis of (3′R)-2′,3′-dideoxy-3′-hydroxymethyl nucleosides

Abstract

Methanol and propan-2-ol add in a regiospecific and highly stereocontrolled fashion to 5-substituted 2,5-dihydrofuran-2-ones (butenolides) under irradiation. The photoadducts with methanol have been converted into a number of (3′R)-2′,3′-dideoxy-3′-hydroxymethyl nucleosides.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 3141-3148

Photocatalysed addition of alcohols to 5-substituted 2,5-dihydrofuran-2-ones: novel synthesis of (3′R)-2′,3′-dideoxy-3′-hydroxymethyl nucleosides

J. Mann and A. C. Weymouth-Wilson, J. Chem. Soc., Perkin Trans. 1, 1994, 3141 DOI: 10.1039/P19940003141

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