Rebecca M. Myers

Affiliations: 
University of Cambridge, Cambridge, England, United Kingdom 
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"Rebecca Myers"
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Parents

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Anthony GM Barrett research assistant 1997-
Christopher Abell grad student 1997-2001
Steven Victor Ley post-doc 2001-
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Publications

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Ley SV, Fitzpatrick DE, Myers RM, et al. (2015) Machine-Assisted Organic Synthesis. Angewandte Chemie (International Ed. in English). 54: 10122-36
Ley SV, Fitzpatrick DE, Ingham RJ, et al. (2015) Organic synthesis: march of the machines. Angewandte Chemie (International Ed. in English). 54: 3449-64
Myers RM, Fitzpatrick DE, Turner RM, et al. (2014) Flow chemistry meets advanced functional materials. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 12348-66
Watts CA, Richards FM, Bender A, et al. (2013) Design, synthesis, and biological evaluation of an allosteric inhibitor of HSET that targets cancer cells with supernumerary centrosomes. Chemistry & Biology. 20: 1399-410
Beale TM, Allwood DM, Bender A, et al. (2012) A-ring dihalogenation increases the cellular activity of combretastatin-templated tetrazoles. Acs Medicinal Chemistry Letters. 3: 177-81
Beale TM, Bond PJ, Brenton JD, et al. (2012) Increased endothelial cell selectivity of triazole-bridged dihalogenated A-ring analogues of combretastatin A-1. Bioorganic & Medicinal Chemistry. 20: 1749-59
Myers RM, Roper KA, Baxendale IR, et al. (2012) The Evolution of Immobilized Reagents and their Application in Flow Chemistry for the Synthesis of Natural Products and Pharmaceutical Compounds Modern Tools For the Synthesis of Complex Bioactive Molecules. 359-393
Qi X, Loiseau F, Chan WL, et al. (2011) Allosteric modulation of hormone release from thyroxine and corticosteroid-binding globulins. The Journal of Biological Chemistry. 286: 16163-73
Shearman JW, Myers RM, Brenton JD, et al. (2011) Total syntheses of subereamollines A and B. Organic & Biomolecular Chemistry. 9: 62-5
Beale TM, Myers RM, Shearman JW, et al. (2010) Antivascular and anticancer activity of dihalogenated A-ring analogues of combretastatin A-4 Medchemcomm. 1: 202-208
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