Fragment-based and structure-guided discovery of perforin inhibitors von Jose, Jiney, Law, Ruby H.P., Leung, Eleanor W.W., Wai, Dorothy C.C., Akhlaghi, Hedieh, Chandrashekaran, Indu R., Caradoc-Davies, Tom T., Voskoboinik, Ilia, Feutrill, John, Middlemiss, David, Jeevarajah, Devadharshini, Bashtannyk-Puhalovich, Tanya, Giddens, Anna C., Lee, Tet Woo, Jamieson, Stephen M.F., Trapani, Joseph A., Whisstock, James C., Spicer, Julie A., Norton, Raymond S.

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Highly Efficient Enantioselective Pauson-Khand Reactions von Hay, Alistair M, Kerr, William J, Kirk, George G, Middlemiss, David

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Indole-3-acetic Acid Antagonists of the Prostaglandin D 2 Receptor CRTH2 von Armer, Richard E., Ashton, Mark R., Boyd, Edward A., Brennan, Chris J., Brookfield, Frederick A., Gazi, Lucien, Gyles, Shân L., Hay, Philip A., Hunter, Michael G., Middlemiss, David, Whittaker, Mark, Xue, Luzheng, Pettipher, Roy

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Indole-3-acetic Acid Antagonists of the Prostaglandin D2 Receptor CRTH2 von Armer, Richard E, Ashton, Mark R, Boyd, Edward A, Brennan, Chris J, Brookfield, Frederick A, Gazi, Lucien, Gyles, Shân L, Hay, Philip A, Hunter, Michael G, Middlemiss, David, Whittaker, Mark, Xue, Luzheng, Pettipher, Roy

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A convenient procedure for the solution phase preparation of 2-aminothiazole combinatorial libraries von Bailey, Nicholas, Dean, Anthony W., Judd, Duncan B., Middlemiss, David, Storer, Richard, Watson, Stephen P.

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Enantioselective Pauson-Khand Reactions Mediated by a Chiral Amine N-Oxide von Kerr, William J., Kirk, George G., Middlemiss, David

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Promotion of the Pauson-Khand Reaction using High Intensity Ultrasound von Ford, J. Gair, Kerr, William J., Kirk, George G., Lindsay, David M., Middlemiss, David

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Tricarbonylchromium(O) promoted stereoselective transformations of ephedrine and pseudoephedrine derivatives von COOTE, S. J, DAVIES, S. G, GOODFELLOW, C. L, SUTTON, K. H, MIDDLEMISS, D, NAYLOR, A

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ANILINE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION von MIDDLEMISS, DAVID, FEUTRILL, JOHN, LERICHE, CAROLINE

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Total synthesis of parvaquone and the serendipitous discovery of a novel chromium-mediated method for β-lactone formation von Harrity, Joseph P.A., Kerr, William J., Middlemiss, David, Scott, James S.

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A direct method for the substitution of imidazo[1,5-a]pyridines at position 5 von Blatcher, Philip, Middlemiss, David

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A medicinal chemistry case study: An account of an angiotensin II antagonist drug discovery programme von Middlemiss, David, Watson, Stephen P.

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biarlamidas von David Middlemiss, Robert Coleman

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HETEROCYCLIC COMPOUNDS, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION von MIDDLEMISS, David, LERICHE, Caroline

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COMPUESTOS HETEROCÌCLICOS, SU PREPARACIÒN Y SU APLICACIÒN TERAPÈUTICA von CAROLINE LERICHE, DAVID MIDDLEMISS

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Heterocyclic compounds, their preparation and their therapeutic application von Leriche Caroline, Middlemiss David

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Chromium-mediated β-lactone synthesis using ultrasonication von Caldwell, John J., Harrity, Joseph P.A., Heron, Nicola M., Kerr, William J., McKendry, Sharon, Middlemiss, David

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Aniline derivatives,their preparation and their therapeutic application von Feutrill, John, Leriche, Caroline, Middlemiss, David

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BIARYLDERIVATIVES,THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION von LERICHE, Caroline, MIDDLEMISS, David, FEUTRILL, John

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A Convenient Synthesis of 4-Oxo-1,2,3,4,4a,9a-hexahydrofluorene and 4-Oxotetrahydrofluorenes von Middlemiss, David

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