Rhenium-catalysed reactions in chemical synthesis: selected case studies

This Perspective presents and discusses a selection of examples that reinforce the enabling and distinctive reactivity provided by homogeneous rhenium catalysis in chemical synthesis. Specifically, the ability for lower oxidation state rhenium-carbonyl catalysts to engage alkyne, allene, and enol substrates in various carbon-carbon bond-forming reactions is highlighted. The inherent capacity of Lewis acidic, higher oxidation state oxorhenium catalysts to facilitate the transposition/isomerisation of allyl alcohols and attendant functionalisation via reaction cascades is also showcased. A brief overview of representative rhenium catalysts that have allowed for reductions of imines, carbonyls, and related compounds is also provided.

Automated summary

This Perspective discusses the importance of homogeneous rhenium catalysis in chemical synthesis, highlighting the reactivity of different oxidation state rhenium catalysts in carbon-carbon bond-forming reactions, transposition/isomerization of allyl alcohols, and reductions of imines and carbonyls.