Issue 0, 1981

Reaction of vinyl sulphone with α-metallated nitriles

Abstract

Vinyl sulphones (1) were subjected to nucleophilic addition by α-lithionitriles (2) and gave cyclized products, 3-oxothian 1,1-dioxides (3) or cyclopropane derivatives (4), in satisfactory yields according to the substituents on the reagents. The cyclopropanation reactions could be extended to the formation of cyclopropyl sulphides (12)–(16) in good yields.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1981, 751-755

Reaction of vinyl sulphone with α-metallated nitriles

T. Agawa, Y. Yoshida, M. Komatsu and Y. Ohshiro, J. Chem. Soc., Perkin Trans. 1, 1981, 751 DOI: 10.1039/P19810000751

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