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. 2007;46(39):7364-76.
doi: 10.1002/anie.200604774.

Enantiomerically enriched cyclopropene derivatives: versatile building blocks in asymmetric synthesis

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Enantiomerically enriched cyclopropene derivatives: versatile building blocks in asymmetric synthesis

Ilan Marek et al. Angew Chem Int Ed Engl. 2007.

Abstract

Enantiomerically enriched cyclopropene derivatives, the smallest possible unsaturated carbocycles, are of great synthetic interest since they serve as versatile reactive building blocks. Their reactivity results from the relief of the ring strain in the small molecule. They can be transformed into a wide variety of complex chiral structures and a special emphasis will be directed towards the preparation of enantiomerically enriched methylene- and alkylidenecyclopropane derivatives. The ready availability of a wide range of these chiral entities now provides an excellent opportunity to discover new and unique transformations that can further enrich mainstream synthetic methodology.

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