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The reaction of conjugated ene-yne-ketones 3 with a variety of alkenes in the presence of a catalytic amount of Cr(CO)(5)(THF) at room temperature gives (2-furyl)cyclopropanes in good yields. These cyclopropanation reactions proceed via (2-furyl)carbene-chromium intermediates 4 formed in situ from ene-yne-ketones 3. Late transition metals, such as RuCl(2)(CO)(3)(2), RhCl(cod)(2), PdCl(2), and PtCl(2), also catalyze effectively the cyclopropanation of styrene with 3.
Miki et al. (Sat,) studied this question.