4.8 Article

Chiral Cyclometalated Oxazoline Gold(III) Complex-Catalyzed Asymmetric Carboalkoxylation of Alkynes

Journal

ORGANIC LETTERS
Volume 21, Issue 16, Pages 6289-6294

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02171

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Funding

  1. Hong Kong Research Grants Council [PolyU 153006/15P]
  2. State Key Laboratory of Chemical Biology and Drug Discovery
  3. Department of Applied Biology and Chemical Technology

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Asymmetric catalysis by using novel chiral O,O'-chelated 4,4'-biphenol cyclometalated oxazoline gold(III) complexes has been developed. A high yield (<= 89%) and a high enantioselectivity (<= 90% ee) were achieved in asymmetric carboalkoxylation of alkynes. Enantioselectivity could be significantly improved from 19% to 90% ee by increasing the steric size of the substituent on the chiral oxazoline ligand. Catalytically active Au-III species and the origin of chiral induction are proposed.

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