Issue 3, 1986

Lewis acid promoted additions of cyclopropanes to iminium salts: a new possibility for α-methylene-γ-butyrolactone synthesis

Abstract

Methyl 2-siloxycyclopropanecarboxylates (1) smoothly add to dimethylmethyleneammonium trifluoromethanesulphonate, generated in situ, or to the corresponding minium chloride (4) in the presence of TiCl4, giving α-aminomethylated γ-oxoesters (6) in good yield; these can serve as precursors for α-methylene-γ-butyrolactones (7) as well as for acrylic ester derivatives (8).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 269-271

Lewis acid promoted additions of cyclopropanes to iminium salts: a new possibility for α-methylene-γ-butyrolactone synthesis

H. Reissig and H. Lorey, J. Chem. Soc., Chem. Commun., 1986, 269 DOI: 10.1039/C39860000269

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