α‑C–H Functionalization of π‑Bonds Using Iron Complexes: Catalytic Hydroxyalkylation of Alkynes and Alkenes
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The discovery of catalytic systems based on earth-abundant transition metals for the functionalization of C–H bonds enables streamlined and sustainable solutions to problems in synthetic organic chemistry. In this Communication, we disclose an iron-based catalytic system for the functionalization of propargylic and allylic C–H bonds. Inexpensive and readily available cyclopentadienyliron(II) dicarbonyl complexes were employed as catalysts for a novel deprotonative activation mode for C–H functionalization, an approach that allows for the direct union of unsaturated building blocks with aryl aldehydes and other carbonyl electrophiles to deliver a range of unsaturated alcohol coupling products under operationally simple and functional group tolerant reaction conditions.



