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• W2101461330 startingPage "6332" @default.
• W2101461330 abstract "In addition to their utility in Barton-McCombie deoxygenations, xanthates can engage in 5-exo-trig radical cyclizations to afford lactones after oxidative workup. In this paper, we describe a tin-free protocol that provides direct access to lactones via hydrolysis of labile thioketal intermediates. Analysis of several systems of varying complexity reveals that the reaction is most applicable for constrained systems in which the reacting center is prepositioned near the radical-accepting alkene." @default.
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• W2101461330 date "2012-07-05" @default.
• W2101461330 modified "2023-10-18" @default.
• W2101461330 title "Xanthates as Synthetic Equivalents of Oxyacyl Radicals: Access to Lactones under Tin-Free Conditions" @default.
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• W2101461330 doi "https://doi.org/10.1021/jo300939f" @default.
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