One-pot consecutive reactions based on the synthesis of conjugated enones by the re-catalysed meyer-schuster rearrangement

Re catalysis in one-pot reactions: An atom-economical, one-pot strategy that involves alkyne deprotonation and a subsequent rhenium(V)-catalysed Meyer-Schuster rearrangement of the alkynol to provide α,?-unsaturated enones in high yield has been developed. Subsequent in situ hydride reduction or Diels-Alder reaction of the enones provided products in good-to-high overall yields.