Issue 4, 1985

Highly diastereoselective reduction of chiral β-ketosulphoxides under chelation control: application to the synthesis of (R)-(+)-n-hexadecano-1,5-lactone

Abstract

The presence of zinc chloride in the reduction of chiral β-ketosulphoxides with di-isobutylaluminium hydride effects high 1,3-asymmetric induction to give β-hydroxysulphoxides; this method can be successfully applied to the synthesis of optically pure 1,4- or 1,5-lactones.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 211-213

Highly diastereoselective reduction of chiral β-ketosulphoxides under chelation control: application to the synthesis of (R)-(+)-n-hexadecano-1,5-lactone

H. Kosugi, H. Konta and H. Uda, J. Chem. Soc., Chem. Commun., 1985, 211 DOI: 10.1039/C39850000211

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