4.8 Review

Recent advances in enantioselective gold catalysis

Journal

CHEMICAL SOCIETY REVIEWS
Volume 45, Issue 16, Pages 4567-4589

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cs00929d

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Funding

  1. NIHGMS [RO1 GM073932]
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM073932] Funding Source: NIH RePORTER

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Interest in homogeneous gold catalysis has undergone a marked increase. As strong yet air-and moisturetolerant pi-acids, cationic gold(I) complexes have been shown to catalyze diverse transformations of alkenes, alkynes and allenes, opening new opportunities for chemical synthesis. The development of efficient asymmetric variants is required in order to take full advantage of the preparative potential of these transformations. During the last few years, the chemical community has achieved tremendous success in the area. This review highlights the updated progress (2011-2015) in enantioselective gold catalysis. The discussion is classified according to the pi-bonds activated by gold(I), in an order of alkynes, allenes and alkenes. Other gold activation modes, such as sigma-Lewis acid catalyzed reactions and transformations of diazo compounds are also discussed.

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