Issue 19, 1987

Unprecedented reaction of a thiocarbonyl ylide with carbonyl compounds: a novel synthesis of 1,3-oxathiolanes

Abstract

Thioformylium methylide, readily generated from chloromethyl trimethylsilylmethyl sulphide with the aid of fluoride ion, reacts with carbonyl compounds such as aldehydes, α-diketones, and α-oxo amides to give the corresponding 1,3-oxathiolanes in good yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1442-1443

Unprecedented reaction of a thiocarbonyl ylide with carbonyl compounds: a novel synthesis of 1,3-oxathiolanes

A. Hosomi, S. Hayashi, K. Hoashi, S. Kohra and Y. Tominaga, J. Chem. Soc., Chem. Commun., 1987, 1442 DOI: 10.1039/C39870001442

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