Metal-Catalyzed Rearrangement of enantiomerically Pure Alkylidenecyclopropane Derivatives as a New access to Cyclobutenes Possessing Quaternary stereocenters

Metal-Catalyzed Rearrangement of enantiomerically Pure Alkylidenecyclopropane Derivatives as a New access to Cyclobutenes Possessing Quaternary stereocenters

Abstract:

Pd(II)- and Pt(II)-catalyzed ring-expansion of enantiomerically pure alkylidenecyclopropane derivatives leads to the formation of cyclobutene species with a complete preservation of the stereogenic center.

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Last updated on 04/28/2016