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      High-Productivity Single-Pass Electrochemical Birch Reduction of Naphthalenes in a Continuous Flow Electrochemical Taylor Vortex Reactor

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          Abstract

          We report the development of a single-pass electrochemical Birch reduction carried out in a small footprint electrochemical Taylor vortex reactor with projected productivities of >80 g day –1 (based on 32.2 mmol h –1), using a modified version of our previously reported reactor [ Org. Process Res. Dev. 2021, 25, 7, 1619–1627], consisting of a static outer electrode and a rapidly rotating cylindrical inner electrode. In this study, we used an aluminum tube as the sacrificial outer electrode and stainless steel as the rotating inner electrode. We have established the viability of using a sacrificial aluminum anode for the electrochemical reduction of naphthalene, and by varying the current, we can switch between high selectivity (>90%) for either the single ring reduction or double ring reduction with >80 g day –1 projected productivity for either product. The concentration of LiBr in solution changes the fluid dynamics of the reaction mixture investigated by computational fluid dynamics, and this affects equilibration time, monitored using Fourier transform infrared spectroscopy. We show that the concentrations of electrolyte (LiBr) and proton source (dimethylurea) can be reduced while maintaining high reaction efficiency. We also report the reduction of 1-aminonaphthalene, which has been used as a precursor to the API Ropinirole. We find that our methodology produces the corresponding dihydronaphthalene with excellent selectivity and 88% isolated yield in an uninterrupted run of >8 h with a projected productivity of >100 g day –1.

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          Escape from flatland: increasing saturation as an approach to improving clinical success.

          The medicinal chemistry community has become increasingly aware of the value of tracking calculated physical properties such as molecular weight, topological polar surface area, rotatable bonds, and hydrogen bond donors and acceptors. We hypothesized that the shift to high-throughput synthetic practices over the past decade may be another factor that may predispose molecules to fail by steering discovery efforts toward achiral, aromatic compounds. We have proposed two simple and interpretable measures of the complexity of molecules prepared as potential drug candidates. The first is carbon bond saturation as defined by fraction sp(3) (Fsp(3)) where Fsp(3) = (number of sp(3) hybridized carbons/total carbon count). The second is simply whether a chiral carbon exists in the molecule. We demonstrate that both complexity (as measured by Fsp(3)) and the presence of chiral centers correlate with success as compounds transition from discovery, through clinical testing, to drugs. In an attempt to explain these observations, we further demonstrate that saturation correlates with solubility, an experimental physical property important to success in the drug discovery setting.
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            Escape from Flatland 2: complexity and promiscuity

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              Transition-metal-mediated dearomatization reactions.

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                Author and article information

                Journal
                Org Process Res Dev
                Org Process Res Dev
                op
                oprdfk
                Organic Process Research & Development
                American Chemical Society
                1083-6160
                1520-586X
                24 August 2022
                16 September 2022
                : 26
                : 9
                : 2674-2684
                Affiliations
                []School of Chemistry, University of Nottingham , University Park, Nottingham NG7 2RD, U.K.
                []Department of Mechanical and Manufacturing Engineering, University of Nottingham , University Park, Nottingham NG7 2RD, U.K.
                [§ ]School of Chemistry, University of Southampton , Highfield, Southampton SO17 1BJ, U.K.
                Author notes
                Author information
                https://orcid.org/0000-0002-8288-1838
                https://orcid.org/0000-0001-6730-3573
                https://orcid.org/0000-0002-7844-1696
                Article
                10.1021/acs.oprd.2c00108
                9486933
                36158467
                f20432fd-0859-40a4-b220-c4320011992f
                © 2022 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 15 April 2022
                Funding
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/P013341/1
                Funded by: University of Nottingham, doi 10.13039/501100000837;
                Award ID: NA
                Categories
                Article
                Custom metadata
                op2c00108
                op2c00108

                birch reduction,electroreduction,electrochemistry,dearomatization,continuous flow,taylor vortex reactor

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