Issue 2, 1973

Synthesis and stereochemistry of bis-(3,4-disubstituted 5-oxo-2,5-dihydrofuran-2-yl) ethers

Abstract

Dehydration of 3,4-disubstituted 5-hydroxyfuran-2(5H)-ones by sulphuric acid or thionyl chloride gave the recemic and meso isomers of the corresponding ethers, bis-(3,4-disubstituted 5-oxo-2,5-dihydrofuran-2-yl) ethers. The stereochemistry of the diastereoisomers has been studied by i.r., u.v., and n.m.r. spectroscopy.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1973, 107-109

Synthesis and stereochemistry of bis-(3,4-disubstituted 5-oxo-2,5-dihydrofuran-2-yl) ethers

S. Kovac, E. Solcaniova, E. Beska and P. Rapos, J. Chem. Soc., Perkin Trans. 2, 1973, 107 DOI: 10.1039/P29730000107

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