Enantioselective Conjugate Allylation of Cyclic Enones
The Journal of Organic Chemistry2011Vol. 76(18), pp. 7614–7617
Citations Over TimeTop 25% of 2011 papers
Abstract
Enantioselective organocatalytic 1,2-allylation of a cyclic enone followed by anionic oxy-Cope rearrangement delivered the ketone as a mixture of diastereomers. This appears to be a general method for the net enantioselective conjugate allylation of cyclic enones.
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