Purins, MikusWaser, Jerome2022-02-142022-02-142022-02-142022-02-0110.1002/anie.202113925https://infoscience.epfl.ch/handle/20.500.14299/185290WOS:000748903100001For the enantioselective diversification of a single starting material, a different chiral catalyst is usually required for each transformation. Herein, we extend the concept of catalytically formed chiral auxiliary from hydrogenation to the asymmetric cyclopropanation and epoxidation of tetra-substituted olefins, alleviating the need for different chiral catalysts in the alkene functionalization step. The chiral auxiliary is catalytically constructed from propargylic amines in a Pd-catalyzed enantioselective carboetherification step using a commercially available trifluoroacetaldehyde hemiacetal tether. The installed auxiliary is then controlling the stereochemistry of the cyclopropanation and the epoxidation using standard highly reactive reagents to give enantioenriched spirocyclic aminomethylcyclopropanols and alpha-amino-alpha-hydroxy ketones.Chemistry, MultidisciplinaryChemistryasymmetric synthesiscyclopropanationcyclopropanolepoxidationrubottom oxidationsilyl enol etherssimmons-smith cyclopropanation3,4-homotropilidenetautomerizationrearrangementsoxidationligandstext::journal::journal article::research article