Abstract
AbstractCyclopropane‐containing amino acids are important pharmaceuticals and biologically active compounds. A new organocatalytic asymmetric Michael reaction has been developed. This allows the one‐step introduction of the cyclopropane ring, as well as two different nitrogen‐containing functional groups (tert‐butoxycarbonylamino and nitro) into the target compounds. All the products were isolated in good yields with moderate to excellent enantio‐ and diastereoselectivities.
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