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      Chiral 1,2-Diaminocyclohexane-α-Amino Acid-Derived Amidphos/Ag(I)-Catalyzed Divergent Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides

      , , , , ,
      HETEROCYCLES
      The Japan Institute of Heterocyclic Chemistry

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          Analysis of the structural diversity, substitution patterns, and frequency of nitrogen heterocycles among U.S. FDA approved pharmaceuticals.

          Nitrogen heterocycles are among the most significant structural components of pharmaceuticals. Analysis of our database of U.S. FDA approved drugs reveals that 59% of unique small-molecule drugs contain a nitrogen heterocycle. In this review we report on the top 25 most commonly utilized nitrogen heterocycles found in pharmaceuticals. The main part of our analysis is divided into seven sections: (1) three- and four-membered heterocycles, (2) five-, (3) six-, and (4) seven- and eight-membered heterocycles, as well as (5) fused, (6) bridged bicyclic, and (7) macrocyclic nitrogen heterocycles. Each section reveals the top nitrogen heterocyclic structures and their relative impact for that ring type. For the most commonly used nitrogen heterocycles, we report detailed substitution patterns, highlight common architectural cores, and discuss unusual or rare structures.
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            Asymmetric enamine catalysis.

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              Enantioselective copper-catalyzed 1,3-dipolar cycloadditions.

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                Author and article information

                Journal
                HTCYAM
                HETEROCYCLES
                HETEROCYCLES
                The Japan Institute of Heterocyclic Chemistry
                0385-5414
                2022
                2022
                : 104
                : 1
                : 123
                Article
                10.3987/COM-21-14561
                b1343bb5-8482-44b4-87af-9a2f67a07414
                © 2022
                History

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