Issue 9, 1994

Aldol reaction of enol acetates and lactols with N-chlorosuccinimide and tin(II) chloride. Diastereoselective synthesis of disubstituted cyclic ethers

Abstract

Lactols reacted with enol acetates by a Lewis acid reagent, derived from N-chlorosuccinimide and tin(II) chloride, to produce 2-acetonyl cyclic ethers diastereoselectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 1123-1123

Aldol reaction of enol acetates and lactols with N-chlorosuccinimide and tin(II) chloride. Diastereoselective synthesis of disubstituted cyclic ethers

Y. Masuyama, Y. Kobayashi and Y. Kurusu, J. Chem. Soc., Chem. Commun., 1994, 1123 DOI: 10.1039/C39940001123

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