A boron-oxygen transborylation strategy for a catalytic Midland reduction

Kieran Nicholson, Joanne Dunne, Peter DaBell, Alexander Beaton Garcia, Andrew D. Bage, Jamie H. Docherty, Thomas A. Hunt, Thomas Langer, Stephen P. Thomas*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

The enantioselective hydroboration of ketones is a textbook reaction requiring stoichiometric amounts of an enantioenriched borane, with the Midland reduction being a seminal example. Here, a turnover strategy for asymmetric catalysis, boron-oxygen transborylation, has been developed and used to transform the stoichiometric borane reagents of the Midland reduction into catalysts. This turnover strategy was demonstrated by the enantioselective reduction of ketones, including derivatives of biologically active molecules and those containing reducible groups. The enantioenriched borane catalyst was generated in situ from commercially available reagents, 9-borabicyclo[3.3.1]nonane (H-B-9-BBN) and β-pinene, and B-O transborylation with pinacolborane (HBpin) was used for catalytic turnover. Mechanistic studies indicated that B-O transborylation proceeded by B-O/B-H boron exchange through a stereoretentive, concerted transition state, resembling σ-bond metathesis.

Original languageEnglish
Pages (from-to)2034-2040
Number of pages7
JournalACS Catalysis
Issue number4
Early online date1 Feb 2021
Publication statusE-pub ahead of print - 1 Feb 2021

Keywords / Materials (for Non-textual outputs)

  • Asymmetric catalysis
  • Boron
  • Enantioselective
  • Hydroboration
  • Ketone
  • Main group
  • Reduction
  • Transborylation


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