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Showing 1 to 5 of 5 for “"Sulfinimines"”.

  1. Asymmetric Synthesis of 1,3-Amino Alcohols and Tropinone Derivatives From Enantiopure Sulfinimines

    … and tropane-containing derivatives using sulfinimines (N-sulfinyl imines) as precursors for acid-catalyzed cascade cyclizations. Chiral N-sulfinyl b-amino ketones derived from N-sulfinyl b-amino Weinreb amides, serve as novel and direct precursors to syn and anti N-sulfinyl 1,3-amino …

    temple Repository record for Asymmetric Synthesis of 1,3-Amino Alcohols and Tropinone Derivatives From Enantiopure Sulfinimines (opens in a new tab)

  2. Asymmetric Synthesis of Homotropinone and Tropane Alkaloids using Enantiopure Sulfinimines and the Synthesis and Applications of Methanoprolines

    … and tropane alkaloids using enantiopure sulfinimines [RS(O)N=CR1R²] is the primary objective of this thesis. In one study a four-step intramolecular Mannich cyclization cascade reaction was devised for the asymmetric synthesis of substituted homotropinone alkaloids from enantiopure …

    temple Repository record for Asymmetric Synthesis of Homotropinone and Tropane Alkaloids using Enantiopure Sulfinimines and the Synthesis and Applications of Methanoprolines (opens in a new tab)

  3. Asymmetric Synthesis of Nitrogen Containing Bioactive Compounds via the Utilization of Enantiopure p-Toluenesulfinimines

    … synthesis of amine derivatives using p-toluenesulfinimines. Enantiopure sulfinimines are versatile chiral building blocks for the asymmetric synthesis of alkaloids. Sulfinimines were prepared by the condensation of (S)- or (R)-p-toluenesulfinamide with aldehydes and ketones in good to excellent …

    temple Repository record for Asymmetric Synthesis of Nitrogen Containing Bioactive Compounds via the Utilization of Enantiopure p-Toluenesulfinimines (opens in a new tab)

  4. Development of new synthetic methodologies

    … to direct the chirality of products. Chiral sulfinimines are successfully utilized as electrophilic acceptors for the asymmetric synthesis of multifunctionalized Baylis- Hillman adducts, p-halo, p-monosubstituted, and p,p-disubstituted Baylis-Hillman olefines. Among these products, …

    tdl Repository record for Development of new synthetic methodologies (opens in a new tab)