Issue 1, 1989

Radical cyclisation of some unsaturated carbohydrate derived acetals

Abstract

Haloacetals derived from pyranosidic allylic alcohols or allylic hemiacetals were stereospecifically cyclized using tributyltin hydride as radical promotor to give fused furanoses; the reaction was also applied to a propargylic glycoside which cyclized readily into a vinylstannane, precursor of methylene furanose.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 39-40

Radical cyclisation of some unsaturated carbohydrate derived acetals

Y. Chapleur and N. Moufid, J. Chem. Soc., Chem. Commun., 1989, 39 DOI: 10.1039/C39890000039

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