Novel heterocyclic DPP-4 inhibitors for the treatment of type 2 diabetes von Sutton, Jon M., Clark, David E., Dunsdon, Stephen J., Fenton, Garry, Fillmore, Amanda, Harris, Neil V., Higgs, Chris, Hurley, Chris A., Krintel, Sussie L., MacKenzie, Robert E., Duttaroy, Alokesh, Gangl, Eric, Maniara, Wiesia, Sedrani, Richard, Namoto, Kenji, Ostermann, Nils, Gerhartz, Bernd, Sirockin, Finton, Trappe, Jörg, Hassiepen, Ulrich, Baeschlin, Daniel K.

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Discovery of C-(1-aryl-cyclohexyl)-methylamines as selective, orally available inhibitors of dipeptidyl peptidase IV von Namoto, Kenji, Sirockin, Finton, Ostermann, Nils, Gessier, Francois, Flohr, Stefanie, Sedrani, Richard, Gerhartz, Bernd, Trappe, Jörg, Hassiepen, Ulrich, Duttaroy, Alokesh, Ferreira, Suzie, Sutton, Jon M., Clark, David E., Fenton, Garry, Beswick, Mandy, Baeschlin, Daniel K.

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Selective Type IV Phosphodiesterase Inhibitors as Antiasthmatic Agents. The Syntheses and Biological Activities of 3-(Cyclopentyloxy)-4-methoxybenzamides and Analogs von Ashton, Michael J, Cook, David C, Fenton, Garry, Karlsson, Jan-Anders, Palfreyman, Malcolm N, Raeburn, David, Ratcliffe, Andrew J, Souness, John E, Thurairatnam, Suga, Vicker, Nigel

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Chemoselective oxidative debenzylation of tertiary N-benzyl amines von Bull, Steven D., Davies, Stephen G., Mulvaney, Andrew W., Prasad, R. Shyam, Smith, Andrew D., Fenton, Garry

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Iodoetherification of homoallylic alcohols : A stereoselective approach to tetrahydrofurans von Bedford, Simon B., Bell, Kathryn E., Fenton, Garry, Hayes, Christopher J., Knight, David W., Shaw, Duncan

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Erratum to “Novel heterocyclic DPP-4 inhibitors for the treatment of type 2 diabetes” [Bioorg. Med. Chem. Lett. 22 (2012) 1464–1468] von Sutton, Jon M., Clark, David E., Dunsdon, Stephen J., Fenton, Garry, Fillmore, Amanda, Harris, Neil V., Higgs, Chris, Hurley, Chris A., Krintel, Sussie L., MacKenzie, Robert E., Duttaroy, Alokesh, Gangl, Eric, Maniara, Wiesia, Sedrani, Richard, Namoto, Kenji, Ostermann, Nils, Gerhartz, Bernd, Sirockin, Finton, Trappe, Jörg, Hassiepen, Ulrich, Baeschlin, Daniel K.

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The Asymmetric Synthesis of β-Haloaryl-β-Amino Acid Derivatives von Bull, Steven D., Davies, Stephen G., Delgado-Ballester, Santiago, Fenton, Garry, Kelly, Peter M., Smith, Andrew D.

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Structure based design of 4-(3-aminomethylphenyl)piperidinyl-1-amides: novel, potent, selective, and orally bioavailable inhibitors of βII tryptase von Levell, Julian, Astles, Peter, Eastwood, Paul, Cairns, Jennifer, Houille, Olivier, Aldous, Suzanne, Merriman, Gregory, Whiteley, Brian, Pribish, James, Czekaj, Mark, Liang, Guyan, Maignan, Sebastien, Guilloteau, Jean-Pierre, Dupuy, Alain, Davidson, Jane, Harrison, Trevor, Morley, Andrew, Watson, Simon, Fenton, Garry, McCarthy, Clive, Romano, Joseph, Mathew, Rose, Engers, Darren, Gardyan, Michael, Sides, Keith, Kwong, Jennifer, Tsay, Joseph, Rebello, Sam, Shen, Liduo, Wang, Jie, Luo, Yongyi, Giardino, Odessa, Lim, Heng-Keang, Smith, Keith, Pauls, Henry

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Mapping the kinase domain of janus kinase 3 von Adams, Christopher, Aldous, David J., Amendola, Shelley, Bamborough, Paul, Bright, Colin, Crowe, Sarah, Eastwood, Paul, Fenton, Garry, Foster, Martyn, Harrison, Trevor K.P., King, Sue, Lai, Justine, Lawrence, Christopher, Letallec, Jean-Philippe, McCarthy, Clive, Moorcroft, Neil, Page, Kenneth, Rao, Sudha, Redford, Jane, Sadiq, Shazia, Smith, Keith, Souness, John E., Thurairatnam, Sukanthini, Vine, Mark, Wyman, Barry

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Total syntheses of natural (+)-(4R,6R)-4-hydroxy-6-pentylvalerolactone and of (-)-(6R)-massoialactone von BENNETT, F, KNIGHT, D. W, FENTON, G

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COMPOSITE PANEL EDGE TREATMENTS AND JOINTS AND CARGO BODY HAVING SAME von FENTON, GARRY L

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COMPOSITE PANEL EDGE TREATMENTS AND JOINTS AND CARGO BODY HAVING SAME von FENTON, GARRY L

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Chemoselective debenzylation of N-benzyl tertiary amines with ceric ammonium nitrate von Bull, Steven D., Davies, Stephen G., Fenton, Garry, Mulvaney, Andrew W., Prasad, R. Shyam, Smith, Andrew D.

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Structure based design of 4-(3-aminomethylphenyl)piperidinyl-1-amides: novel, potent, selective, and orally bioavailable inhibitors of betaII tryptase von Levell, Julian, Astles, Peter, Eastwood, Paul, Cairns, Jennifer, Houille, Olivier, Aldous, Suzanne, Merriman, Gregory, Whiteley, Brian, Pribish, James, Czekaj, Mark, Liang, Guyan, Maignan, Sebastien, Guilloteau, Jean-Pierre, Dupuy, Alain, Davidson, Jane, Harrison, Trevor, Morley, Andrew, Watson, Simon, Fenton, Garry, McCarthy, Clive, Romano, Joseph, Mathew, Rose, Engers, Darren, Gardyan, Michael, Sides, Keith, Kwong, Jennifer, Tsay, Joseph, Rebello, Sam, Shen, Liduo, Wang, Jie, Luo, Yongyi, Giardino, Odessa, Lim, Heng-Keang, Smith, Keith, Pauls, Henry

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Mapping the kinase domain of Janus Kinase 3: Recent advances in the design of kinase inhibitors as novel therapeutic agents von ADAMS, Christopher, ALDOUS, David J, KING, Sue, LAI, Justine, LAWRENCE, Christopher, LETALLEC, Jean-Philippe, MCCARTHY, Clive, MOORCROFT, Neil, PAGE, Kenneth, RAO, Sudha, REDFORD, Jane, SADIQ, Shazia, AMENDOLA, Shelley, SMITH, Keith, SOUNESS, John E, THURAIRATNAM, Sukanthini, VINE, Mark, WYMAN, Barry, BAMBOROUGH, Paul, BRIGHT, Colin, CROWE, Sarah, EASTWOOD, Paul, FENTON, Garry, FOSTER, Martyn, HARRISON, Trevor K. P

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An Asymmetric Synthesis of Muscarine, Suitable for the Elaboration of 5- Substituted Analogues von Knight, David W., Shaw, Duncan, Fenton, Garry

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SUBSTITUTED ALKANOIC ACIDS von FENTON, GARRY, HARRIS, NEIL VICTOR

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SUBSTITUTED TETRAHYDROISOQUINOLINES FOR USE IN THE TREATMENTOF INFLAMMATORY DISEASES von FENTON, GARRY, HARRIS, NEIL VICTOR

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Synthesis of conformationally restricted relatives of the mevinic acids von Bennett, Frank, Fenton, Garry, W. Knight, David

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Hypolipidemic 2-[4-(1,1-dimethylethyl)phenyl]-4H-3,1-benzoxazin-4-ones. Structure-activity relationships of a novel series of high-density lipoprotein elevators von Fenton, Garry, Newton, Christopher G, Wyman, Barry M, Bagge, Philip, Dron, Donald I, Riddell, David, Jones, Graham D

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