Synthesis and Reactivity of 1,2-Dioxolanes from β,γ-Epoxy Ketones
收藏NIAID Data Ecosystem2026-03-08 收录
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Five-membered ring peroxides were prepared in one step in 31–86% yield from readily accessible β,γ-epoxy ketones and H2O2. The reaction proceeded via a tetrahydrofuran, which was converted to the thermodynamically favored 1,2-dioxolane. The product contains a leaving group, which can be displaced to synthesize analogues of the plakinic acid natural products.
创建时间：
2014-05-16
