Issue 19, 1984

Chiral cyclohexanes from carbohydrates: successful carbocyclisation of a D-arabino-hex-5-enopyranoside derivative

Abstract

Carbocyclisation of a hex-5-enopyranoside of D-arabino configuration under modified Ferrier's conditions gave chiral substituted cyclohexanes, which are precursors of aminocyclitols and useful synthetic intermediates, in good yield and without side reactions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1268-1269

Chiral cyclohexanes from carbohydrates: successful carbocyclisation of a D-arabino-hex-5-enopyranoside derivative

F. Chretien and Y. Chapleur, J. Chem. Soc., Chem. Commun., 1984, 1268 DOI: 10.1039/C39840001268

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