Kinetic Resolution of Racemic 2-Hydroxyamides Using a Diphenylacetyl Component as an Acyl Source and a Chiral Acyl-Transfer Catalyst

  • Takatsugu Murata
  • Tatsuya Kawanishi
  • Akihiro Sekiguchi
  • Ryo Ishikawa
  • Keisuke Ono
  • Kenya Nakata
  • Isamu Shiina
Publication date
August 2018
Publisher
MDPI AG
ISSN
1420-3049
Journal
Molecules

Abstract

Various optically active 2-hydroxyamide derivatives are produced based on the kinetic resolution of racemic 2-hydroxyamides with a diphenylacetyl component and (R)-benzotetramisole ((R)-BTM), a chiral acyl-transfer catalyst, via asymmetric esterification and acylation. It was revealed that a tertiary amide can be used with this novel protocol to achieve high selectivity (22 examples; s-value reaching over 250). The resulting chiral compounds could be transformed into other useful structures while maintaining their chirality

Extracted data

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