Highly Regio‑, Diastereo‑, and Enantioselective Rhodium-Catalyzed Intramolecular Cyclopropanation of (<i>Z</i>)‑1,3-Dienyl Aryldiazoacetates

Chiral cyclopenta­[2,3]­cyclopropa­[1,2-c]­pyran-4-ones have been synthesized via dirhodium­(II)-catalyzed intramolecular cyclopropanation of (Z)-1,3-dienyl aryldiazoacetates. High regio-, diastereo-, and enantiocontrol were achieved using chiral dirhodium 2-phthalimide carboxylates. Preferential addition occurs at the 3,4- rather than the 1,2-double bond with the chiral dirhodium catalysts, although both outcomes occur with other transition-metal catalysts.