Synfacts 2006(3): 0244-0244  
DOI: 10.1055/s-2006-932024
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Catalytic Asymmetric Claisen Rearrangement

Contributor(s): Hisashi Yamamoto, Matthew B. Boxer
A. Pollex, M. Hiersemann*
Technische Universität Dresden, Germany
Further Information

Publication History

Publication Date:
21 February 2006 (online)

Significance

Due to the relatively rare synthetic protocols for xenicanes, this progress described by the authors is substantial. Although the catalyst loading is high (25 mol%), the selectivity is essentially perfect (>90% de with >99% ee), making this transformation very useful. Interestingly, the authors found that the geometrical isomer with a Z-double bond (marked blue in the scheme) remains completely unchanged. They attribute this to steric repulsion in the transition state.