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Eddie Myers

Senior Research Associate
Chemistry
Chemical Computing Group
Romania

Biography

    Dr Eddie Myers  is the senior Research Associate in the field of Chemistry.He completed his Master degree from Romania University.  

Research Interest

  Latest publications Armstrong, RJ, García-Ruiz, C, Myers, EL & Aggarwal, VK, 2017, ‘Stereodivergent Olefination of Enantioenriched Boronic Esters’. Angewandte Chemie International Edition, vol 56., pp. 786-790 Fawcett, A, Pradeilles, J, Wang, Y, Mutsuga, T, Myers, EL & Aggarwal, VK, 2017, ‘Photoinduced decarboxylative borylation of carboxylic acids’. Science, vol 357., pp. 283-286 Blair, DJ, Tanini, D, Bateman, JM, Scott, HK, Myers, EL & Aggarwal, VK, 2017, ‘Selective uni- and bidirectional homologation of diborylmethane’. Chemical Science, vol 8., pp. 2898-2903 Aichhorn, S, Bigler, R, Myers, EL & Aggarwal, VK, 2017, ‘Enantiospecific Synthesis of ortho-Substituted Benzylic Boronic Esters by a 1,2-Metalate Rearrangement/1,3-Borotropic Shift Sequence’. Journal of the American Chemical Society, vol 139., pp. 9519-9522 Wu, J, Lorenzo, P, Zhong, S, Ali, M, Butts, CP, Myers, EL & Aggarwal, VK, 2017, ‘Synergy of synthesis, computation and NMR reveals correct baulamycin structures’. Nature, vol 547., pp. 436-440 Fawcett, A, Nitsch, D, Ali, M, Bateman, JM, Myers, EL & Aggarwal, VK, 2016, ‘Regio- and Stereoselective Homologation of 1,2-Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3-Diols and Sch 725674’. Angewandte Chemie International Edition, vol 55., pp. 14663-14667 Casoni, G, Myers, EL & Aggarwal, VK, 2016, ‘Synthesis of 3-Aryl-1-aminopropane Derivatives: Lithiation-Borylation-Ring-Opening of Azetidinium Ions’. Synthesis, vol 48., pp. 3241-3253 Blair, D, Zhong, S, Hesse, M, Zabaleta, N, Myers, E & Aggarwal, V, 2016, ‘Full chirality transfer in the synthesis of hindered tertiary boronic esters under in situ lithiation–borylation conditions’. Chemical Communications, vol 52., pp. 5289-5292 Wang, Y, Noble, A, Myers, EL & Aggarwal, VK, 2016, ‘Enantiospecific Alkynylation of Alkylboronic Esters’. Angewandte Chemie International Edition, vol 55.  

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