Scientific article
English

Creation of Quaternary Stereogenic Centers via Copper-Catalyzed Asymmetric Conjugate Addition of Alkenyl Alanes to α,β-Unsaturated Cyclic Ketones

Published inSynlett, vol. 2010, no. 11, p. 1694-1698
Publication date2010
Abstract

SimplePhos ligands proved to be very powerful ligands in the generation of quaternary stereogenic centers by Michael addition of alkenyl-aluminum reagents to cyclic enones. Using commercially available and easily accessible alkenylbromides as alane precursors the present procedure offers a facile access to β-alkenyl-substituted cyclohexanones with high enantioselectivities up to 96%.

Keywords
  • Aluminum
  • Alkenes
  • Copper
  • Michael addition
  • Asymmetric catalysis
Citation (ISO format)
MÜLLER, Daniel et al. Creation of Quaternary Stereogenic Centers via Copper-Catalyzed Asymmetric Conjugate Addition of Alkenyl Alanes to α,β-Unsaturated Cyclic Ketones. In: Synlett, 2010, vol. 2010, n° 11, p. 1694–1698. doi: 10.1055/s-0029-1219958
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Article (Published version)
accessLevelRestricted
Identifiers
Journal ISSN0936-5214
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Technical informations

Creation28/06/2010 17:51:00
First validation28/06/2010 17:51:00
Update14/03/2023 15:49:31
Status update14/03/2023 15:49:31
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