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A method for the asymmetric construction of functionalized acyclic all‐carbon quaternary stereocenters and 1,3‐nonadjacent stereoelements has been developed via organo/metal dual catalyzed asymmetric allenylic substitution of branched and linear aldehydes, by developing an unknown acyclic secondary‐secondary diamine as the enabling organocatalyst. Although it is believed that secondary‐secondary diamines are difficult to be used as the organocatalysts in organo/metal dual catalysis, this study demonstrates that such diamines can be successfully combined with a metal catalyst in organo/metal dual catalysis. Our study enables the asymmetric construction of two important classes of motifs which were previously difficult to access, axially chiral allene‐containing acyclic all‐carbon quaternary stereocenters and 1,3‐nonadjacent stereoelements bearing allenyl axial chirality and central chirality, in good yields with high enantio‐ and diastereoselectivity. [ABSTRACT FROM AUTHOR]

The first organocatalytic synthesis of terminal propargylic amines from aldehydes via tandem amination/Seyferth-�Gilbert alkynylation has been developed. The described protocol provides the formal addition products of acetylene (HC≡CH) to ali�phatic imines, which are not easily obtained directly. [ABSTRACT FROM AUTHOR]

Abstract: A short review on the development and application of chiral primary amine catalysts in organocatalytic enantioselective reactions has been described. [Copyright &y& Elsevier]

This is the first metal-catalyzed 1,4-selective asymmetric addition of malonates to nitroenynes using a nickel(II)-diamine catalyst. [ABSTRACT FROM AUTHOR]