
GlaxoSmithKline
GlaxoSmithKline
151 Projects, page 1 of 31
assignment_turned_in Project2009 - 2013Partners:GlaxoSmithKline (United Kingdom), University of Oxford, GlaxoSmithKlineGlaxoSmithKline (United Kingdom),University of Oxford,GlaxoSmithKlineFunder: UK Research and Innovation Project Code: BB/G53035X/1Funder Contribution: 72,540 GBPDoctoral Training Partnerships: a range of postgraduate training is funded by the Research Councils. For information on current funding routes, see the common terminology at https://www.ukri.org/apply-for-funding/how-we-fund-studentships/. Training grants may be to one organisation or to a consortia of research organisations. This portal will show the lead organisation only.
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For further information contact us at helpdesk@openaire.euassignment_turned_in Project2011 - 2015Partners:QMUL, GlaxoSmithKline, GlaxoSmithKline Res and DevQMUL,GlaxoSmithKline,GlaxoSmithKline Res and DevFunder: UK Research and Innovation Project Code: BB/I532788/1Funder Contribution: 83,566 GBPDoctoral Training Partnerships: a range of postgraduate training is funded by the Research Councils. For information on current funding routes, see the common terminology at https://www.ukri.org/apply-for-funding/how-we-fund-studentships/. Training grants may be to one organisation or to a consortia of research organisations. This portal will show the lead organisation only.
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For further information contact us at helpdesk@openaire.euassignment_turned_in Project2023 - 2027Partners:GlaxoSmithKline (United Kingdom), GlaxoSmithKline, University of OxfordGlaxoSmithKline (United Kingdom),GlaxoSmithKline,University of OxfordFunder: UK Research and Innovation Project Code: BB/W510567/1Funder Contribution: 112,200 GBPDoctoral Training Partnerships: a range of postgraduate training is funded by the Research Councils. For information on current funding routes, see the common terminology at https://www.ukri.org/apply-for-funding/how-we-fund-studentships/. Training grants may be to one organisation or to a consortia of research organisations. This portal will show the lead organisation only.
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For further information contact us at helpdesk@openaire.euassignment_turned_in Project2007 - 2011Partners:GlaxoSmithKline (United Kingdom), GlaxoSmithKline, KCLGlaxoSmithKline (United Kingdom),GlaxoSmithKline,KCLFunder: UK Research and Innovation Project Code: BB/E528479/1Funder Contribution: 78,820 GBPDoctoral Training Partnerships: a range of postgraduate training is funded by the Research Councils. For information on current funding routes, see the common terminology at https://www.ukri.org/apply-for-funding/how-we-fund-studentships/. Training grants may be to one organisation or to a consortia of research organisations. This portal will show the lead organisation only.
All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=ukri________::101220a923d33a243ffd9b99421ad24d&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eumore_vert All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=ukri________::101220a923d33a243ffd9b99421ad24d&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euassignment_turned_in Project2007 - 2009Partners:University of Oxford, GlaxoSmithKline R & D Ltd, GlaxoSmithKlineUniversity of Oxford,GlaxoSmithKline R & D Ltd,GlaxoSmithKlineFunder: UK Research and Innovation Project Code: EP/E020232/1Funder Contribution: 148,549 GBPThe chemistry in this proposal involves the development of a series of cascade processes based on combinations of C-N, C-O, C-S and C-C coupling reactions, mediated by copper and palladium based catalysts, to deliver a variety of functionalised heterocyclic products. Significant variation of the heterocyclic core and the nature and position of the substituents will be possible employing what is essentially a single strategy. Although the individual reactions used to construct these cascades are well established, it is the ability to combine them in productive processes that will allow valuable drug-like molecules to be produced. Cascades of C-X bond forming reactions offer great potential for heterocycle synthesis as they the introduction of the functional groups and heteroatom combinations frequently encountered in drug-like molecules. Cascade sequences involving up to four bond forming processes will be used to prepare complex, drug-like molecules in a single step. A significant aspect of the chemistry involves demonstrating that it can be applied to array synthesis.
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