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26.3.1.1.1.1 Variation 1: Photodecarbonylation of Cyclobutanediones

DOI: 10.1055/sos-SD-026-00451

Salaün, J.Science of Synthesis, (200526607.

Cyclobutane-1,2-diones, which are readily available from the acyloin condensation of succinic esters followed by bromination, readily undergo photo-induced decarbonylation or water-induced ring contraction.[‌4‌] Thus, the cyclobutane-1,2-dione 2, obtained from the succinate 1 in 55% yield, upon irradiation leads to the cyclopropanone 3 as well as polymeric products (Scheme 1).[‌22‌]

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