Issue 15, 1971

A novel synthesis of benzyl 1,5-dithio-α-and β-L-arabinopyranosides from 5-O-toluene-p-sulphonyl-L-arabinose dibenzyl dithioacetal

Abstract

Benzyl 1,5-dithio-α- and -β-L-arabinopyrano-sides are formed when 5-O-toluene-p-sulphonyl-L-arabinose dibenzyl dithioacetal is heated in acetone containing sodium iodide.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 811-811

A novel synthesis of benzyl 1,5-dithio-α-and β-L-arabinopyranosides from 5-O-toluene-p-sulphonyl-L-arabinose dibenzyl dithioacetal

J. Harness and N. A. Hughes, J. Chem. Soc. D, 1971, 811 DOI: 10.1039/C29710000811

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