Photocatalytic Transfer Hydrogenolysis of Allylic Alcohols on Pd/TiO2 : A Shortcut to (S)-(+)-Lavandulol

Chemistry. 2017 Dec 19;23(71):18025-18032. doi: 10.1002/chem.201704099. Epub 2017 Dec 1.

Abstract

We report herein a regio- and stereoselective photocatalytic hydrogenolysis of allylic alcohols to form unsaturated hydrocarbons employing a palladium(II)-loaded titanium oxide; the reaction proceeds at room temperature under light irradiation without stoichiometric generation of salt wastes. Olefin and saturated alcohol moieties tolerated the reaction conditions. Hydrogen atoms were selectively incorporated into less sterically congested carbons of the allylic functionalities. This protocol allowed a short-step synthesis of (S)-(+)-lavandulol from (R)-(-)-carvone by avoiding otherwise necessary protection/deprotection steps.

Keywords: allylic alcohols; hydrogenolysis; palladium; photocatalysis; titanium oxide.

MeSH terms

  • Acyclic Monoterpenes
  • Alkenes / chemistry
  • Catalysis
  • Cyclohexane Monoterpenes
  • Hydrogenation
  • Light
  • Monoterpenes / chemical synthesis
  • Monoterpenes / chemistry*
  • Palladium / chemistry*
  • Propanols / chemistry*
  • Stereoisomerism
  • Titanium / chemistry*

Substances

  • Acyclic Monoterpenes
  • Alkenes
  • Cyclohexane Monoterpenes
  • Monoterpenes
  • Propanols
  • titanium dioxide
  • allyl alcohol
  • Palladium
  • carvone
  • Titanium
  • lavandulol