Asymmetric Hydroalkoxylation

  • ChemPubSoc Europe Logo
  • Author: Andrea Stomps
  • Published Date: 30 November 2016
  • Source / Publisher: Chemistry – A European Journal/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
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One of the earliest reported gold(I)-catalyzed reactions, the intermolecular hydroalkoxylation of allenes, suffers from poor chirality transfer. This is caused by the rapid racemization of the 1,3-disubstituted allene substrate (example pictured) under the reaction conditions.


Ai-Lan Lee and colleagues, Heriot-Watt University Edinburgh, UK, have investigated reaction conditions (i.e., solvent, temperature, nucleophile, and substrate scope) to improve the chirality transfer for these challenging substrates. They discovered that the use of a coordinating solvent such as dimethylformamide in combination with low temperatures of approximately 0 °C helped to significantly decrease allene racemization. Furthermore, the addition of higher equivalents of alcohol nucleophile (e.g., BnOH) improved the enantiomeric ratio of the hydroalkoxylated products.


A wide variety of allene substrates was tolerated in this reaction, including sterically hindered and acid-sensitive allenes. Some functional groups on the substrate were actually necessary to achieve excellent regioselectivities through inductive withdrawing effects. With this protocol, an excellent chirality transfer of up to 99:1 enantiomeric ratio could be achieved.


 

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