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      Contribution of Organofluorine Compounds to Pharmaceuticals

      review-article
      , , , , § ,
      ACS Omega
      American Chemical Society

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          Abstract

          Inspired by the success of fluorinated corticosteroids in the 1950s and fluoroquinolones in the 1980s, fluorine-containing pharmaceuticals, which are also known as fluoro-pharmaceuticals, have been attracting attention for more than half of a century. Presently, about 20% of the commercial pharmaceuticals are fluoro-pharmaceuticals. In this mini-review, we analyze the prevalence of fluoro-pharmaceuticals in the market and categorize them into several groups based on the chemotype of the fluoro-functional groups, their therapeutic purpose, and the presence of heterocycles and/or chirality to highlight the structural motifs, patterns, and promising trends in fluorine-based drug design. Our database contains 340 fluoro-pharmaceuticals, from the first fluoro-pharmaceutical, Florinef, to the latest fluoro-pharmaceuticals registered in 2019 and drugs that have been withdrawn. The names and chemical structures of all the 340 fluorinated drugs discussed are provided in the Supporting Information.

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          Most cited references19

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          The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates.

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            Synthetic methods for compounds having CF3-S units on carbon by trifluoromethylation, trifluoromethylthiolation, triflylation, and related reactions.

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              Modern Approaches for Asymmetric Construction of Carbon–Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs

              New methods for preparation of tailormade fluorine-containing compounds are in extremely high demand in nearly every sctor of chemical industry. The asymmetric construction of quaternary C−F stereogenic centers is the most synthetically challenging and, consequently, the least developed area of research. As a reflection of this apparent methodological deficit, pharmaceutical drugs featuring C−F stereogenic centers constitute less than 1% of all fluorine-containing medicines currently on the market or in clinical development. Here we provide a comprehensive review of current research activity in this area, including such general directions as asymmetric electrophilic fluorination via organocatalytic and transition-metal catalyzed reactions, asymmetric elaboration of fluorine-containing substrates via alkylations, Mannich, Michael, and aldol additions, cross-coupling reactions, and biocatalytic approaches.

                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                22 April 2020
                19 May 2020
                : 5
                : 19
                : 10633-10640
                Affiliations
                []Sagami Chemical Research Institute , 2743-1 Hayakawa, Ayase, Kanagawa 252-1193, Japan
                []Department of Life Science and Applied Chemistry, Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology , Gokiso, Showa-ku, Nagoya 466-5888, Japan
                [§ ]Institute of Advanced Fluorine-Containing Materials, Zhejiang Normal University , 688 Yingbin Avenue, 321004 Jinhua, China
                Author notes
                Article
                10.1021/acsomega.0c00830
                7240833
                32455181
                c30dde2c-a1c1-4a40-9e80-1e9aa14f00ab
                Copyright © 2020 American Chemical Society

                This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.

                History
                : 25 February 2020
                : 10 April 2020
                Categories
                Mini-Review
                Custom metadata
                ao0c00830
                ao0c00830

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