Journal
ORGANIC LETTERS
Volume 2, Issue 3, Pages 389-391Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol9913441
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[GRAPHICS] Five- to seven-membered lactones were prepared from omega-hydroxyalkyl iodides and CO by atom transfer carbonylation without the need for transition metal catalysts, The reaction proceeds via a hybrid radical/ionic mechanism in which the intramolecular alcoholysis of an omega-hydroxyacyl iodide, arising from atom transfer carbonylation, leads to the lactone.
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