Výsledky vyhledávání - "Wolstenhulme, Jamie R."

Akademický článek

Discovery of a Highly Selective Cell-Active Inhibitor of the Histone Lysine Demethylases KDM2/7.

Autor: Gerken, Philip A.¹, Wolstenhulme, Jamie R.¹, Tumber, Anthony², Hatch, Stephanie B.², Zhang, Yijia¹, Müller, Susanne², Chandler, Shane A.¹, Mair, Barbara², Li, Fengling³, Nijman, Sebastian M. B.², Konietzny, Rebecca², Szommer, Tamas², Yapp, Clarence², Fedorov, Oleg², Benesch, Justin L. P.¹, Vedadi, Masoud³, Kessler, Benedikt M.², Kawamura, Akane¹, Brennan, Paul E.² paul.brennan@sgc.ox.ac.uk, Smith, Martin D.¹ martin.smith@chem.ox.ac.uk

Publikováno v: Angewandte Chemie. 12/4/2017, Vol. 129 Issue 49, p15761-15765. 5p.

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Akademický článek

Asymmetric Electrophilic Fluorocyclization with Carbon Nucleophiles.

Autor: Wolstenhulme, Jamie R.¹, Rosenqvist, Jessica¹, Lozano, Oscar¹, Ilupeju, John¹, Wurz, Nathalie¹, Engle, Keary M.¹, Pidgeon, George W.¹, Moore, Peter R.², Sandford, Graham³, Gouverneur, Véronique¹

Publikováno v: Angewandte Chemie. Sep2013, Vol. 125 Issue 37, p9978-9982. 5p.

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Cation-controlled enantioselective and diastereoselective synthesis of indolines: an autoinductive phase-transfer initiated 5-endo-trig process

Autor: Sharma, Krishna, Wolstenhulme, Jamie R., Painter, Phillip P., Yeo, David, Grande-Carmona, Francisca, Johnston, Craig P., Tantillo, Dean J., Smith, Martin D.

The European Research Council has provided financial support under the European Community’s Seventh Framework Programme (FP7/2007-2013)/ERC grant agreement no. 259056. We are grateful to EPSRC and Pfizer for an award (to CPJ, EP/G041628/1), and the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::81dbf83f28398908d06e3f706311c8d0
https://doi.org/10.1021/jacs.5b08834

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Dissertation/ Thesis

Recent developments in fluorocyclization methodology

Autor: Wolstenhulme, Jamie R.

This thesis has focussed on three main projects, all concerning electrophilic fluorination and fluorocyclization methodology. To begin with we considered the development of a novel fluoro-carbocyclization reaction, which combined the use of substrate

Externí odkaz: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.645961

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