4.7 Article

Enantioselective Allylation of Indoles: A Surprising Diastereoselectivity

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 85, Issue 4, Pages 1894-1905

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.9b02573

Keywords

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Funding

  1. Fonds der Chemischen Industrie
  2. Studienstiftung des Deutschen Volkes
  3. Heinrich-Heine-Universitat Diisseldorf
  4. Forschungszentrum Julich GmbH
  5. University of Cologne
  6. DFG

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Herein we show a novel approach toward the allylation of indoles. Thereby, we explore a class of bench-stable allylboronates and fine-tune their reactivity. The allylations of different substituted indoles proceed with negligible diastereo- and excellent enantioselectivities. This surprising selectivity (up to 99:1 er, up to approximate to 60:40 dr) is rationalized by DFT calculations.

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