Molecules (Aug 2018)

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

DOI
https://doi.org/10.3390/molecules23082003
Journal volume & issue
Vol. 23, no. 8
p. 2003

Abstract

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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.

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