AI Article Synopsis

  • The study introduces a new method for converting primary alcohols or aldehydes into α,β-acetylenic ketones (ynones) using metal catalysis.
  • Deuterium labeling experiments support a unique reaction mechanism where alkyne hydroruthenation creates a temporary vinylruthenium complex.
  • This complex then deprotonates the terminal alkyne, producing a reactive alkynylruthenium nucleophile that drives the reaction.

Article Abstract

The first metal-catalyzed oxidative alkynylations of primary alcohols or aldehydes to form α,β-acetylenic ketones (ynones) are described. Deuterium labelling studies corroborate a novel reaction mechanism in which alkyne hydroruthenation forms a transient vinylruthenium complex that deprotonates the terminal alkyne to form the active alkynylruthenium nucleophile.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213147PMC
http://dx.doi.org/10.1002/anie.202303345DOI Listing

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