Issue 9, 1989

Double Michael addition in the synthesis of tertiary allylic nitro compounds

Abstract

Tertiary allylic vitro compounds have been synthesized in good yields by the double Michael addition of primary nitroalkanes to electron-deficient acetylenes and alkenes in the presence of potassium fluoride and tetrabutylammonium chloride in dimethyl sulphoxide.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 1694-1695

Double Michael addition in the synthesis of tertiary allylic nitro compounds

D. A. Anderson and J. R. Hwu, J. Chem. Soc., Perkin Trans. 1, 1989, 1694 DOI: 10.1039/P19890001694

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