Stereoselective Construction of Methylenecyclobutane-Fused Indolines through Photosensitized [2+2] Cycloaddition of Allene-Tethered Indole Derivatives.

Irradiation of 1-(hexa-4,5-dienoyl)indole derivatives in the presence of an aromatic ketone by a high-pressure mercury lamp through Pyrex glass gave the corresponding cyclized products stereoselectively in high yields. The major part of the products was an all- cis-fused methylenecyclobutane-type compound produced through [2+2] cycloaddition, accompanied by small amounts of alkynes via 1,5-hydrogen transfer of a biradical intermediate. Among a range of aromatic ketones, 3',4'-dimethoxyacetophenone was found to sensitize the substrate quite effectively.