Enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by Ti(IV) complexes of C2-symmetrical chiral BINOL derivatives

Shaohua Gou, Zaher M.A. Judeh*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

37 Citations (Scopus)

Abstract

Enantioselective addition of diethylzinc to a series of aromatic aldehydes is developed using new chiral C2-symmetric ligand (S)-2,2′-(1,1′-binaphthyl-2,2′-diylbis(oxy))bis(methyl ene)bis(4-nitrophenol) (S)-2b. The catalytic system employing 10 mol % of (S)-2b and 120 mol % of Ti(OiPr)4 was found to promote the addition of diethylzinc to a wide range of aromatic aldehydes with electron-donating and electron-withdrawing substituents, giving up to 89% ee and up to 95% yield of the corresponding secondary alcohol under mild conditions.

Original languageEnglish
Pages (from-to)281-283
Number of pages3
JournalTetrahedron Letters
Volume50
Issue number3
DOIs
Publication statusPublished - Jan 21 2009
Externally publishedYes

ASJC Scopus Subject Areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Keywords

  • Aldehyde
  • Alkylation
  • BINOL
  • Chiral C-symmetric ligand
  • Chiral core
  • Diethylzinc
  • Secondary alcohol
  • Ti(OiPr)

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