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Direct Asymmetric Synthesis of β-Bis-Aryl-α-Amino Acid Esters via Enantioselective Copper-Catalyzed Addition of p-Quinone Methides

  • Fu Sheng He
  • , Jing Hai Jin
  • , Zhong Tao Yang
  • , Xingxin Yu
  • , John S. Fossey
  • , Wei Ping Deng*
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

132 Citations (Scopus)

Abstract

A highly efficient synthetic approach to unnatural chiral β-Ar,Ar′-α-amino acid esters bearing two contiguous stereogenic centers has been developed. The first enantioselective 1,6-conjugate addition of glycine Schiff bases to para-quinone methides was achieved using a Cu(CH3CN)4BF4/Ph-Foxap catalytic system (1 mol %). The reaction proceeded smoothly to generate corresponding products in high yields with excellent diastereoselectivities (up to 99:1) and enantioselectivities (up to >99% ee). Subsequent reduction delivered enantiopure unnatural amino alcohols, which were utilized for the synthesis of novel chiral ligands.

Original languageEnglish
Pages (from-to)652-656
Number of pages5
JournalACS Catalysis
Volume6
Issue number2
Early online date23 Dec 2015
DOIs
Publication statusPublished - 28 Dec 2015

Keywords

  • asymmetric catalysis
  • conjugate addition
  • copper
  • para-quinone methides
  • unnatural α-amino acids

ASJC Scopus subject areas

  • Catalysis

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