“…Potassium acetate (Table , entries 6–8) was found to be a better suited base than sodium carbonate (Table , entries 1–5), and in the former case the reaction under nitrogen gave a slightly lower yield of alcohol 3 a than that under air (Table , entries 6 and 8). The lower yield obtained under oxygen atmosphere (Table , entry 2) already indicated at an early stage that radical trapping by oxygen is—in contrast to many other carbooxygenations,—at least not the major mechanistic pathway. The use of twice as much alkene 2 a (12 equivalents) did not further increase the yield, as the reaction was then complicated by phase separation (Table , entry 5).…”