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Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, UK
E-mail: stephen.fletcher@chem.ox.ac.uk
; Tel: +44 (0)18652 75642
Chem. Commun., 2013,49, 4211-4213
DOI:
10.1039/C2CC37155C
Received
01 Oct 2012,
Accepted
19 Nov 2012
First published online
20 Nov 2012
Copper catalysis allows alkyl zirconium species, generated in situ from alkenes, to undergo conjugate addition reactions. A hydrometallation-catalytic asymmetric 1,4-addition was used to synthesize either enantiomer of a natural product in one step from commercially available materials. Hydrometallation-addition sequences applied to steroids containing a cross-conjugated dienone or 1,6-acceptor give highly functionalized products.
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