Issue 7, 1986

Intramolecular C-arylation of benzylated sugars. The unexpected double C-glycosideration of tris-O-m-methoxybenzyl-β-D-ribofuranose derivatives

Abstract

Upon treatment with tin(IV) chloride, D-ribofuranose derivatives bearing activated O-benzyl groups were found to undergo single or double intramolecular C-arylation, with m-methyl- and m-methoxy-substituted benzyl groups respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 497-498

Intramolecular C-arylation of benzylated sugars. The unexpected double C-glycosideration of tris-O-m-methoxybenzyl-β-D-ribofuranose derivatives

O. R. Martin and R. E. Mahnken, J. Chem. Soc., Chem. Commun., 1986, 497 DOI: 10.1039/C39860000497

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