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Page 1
Study of a new rate increasing "base effect" in the palladium-catalyzed amination of aryl iodides.
J Org Chem. 2004 Sep 3;69(18):6010-7. doi: 10.1021/jo049774e.
J Org Chem. 2004.
PMID: 15373485
Synthesis, cytotoxicity, and antiplasmodial and antitrypanosomal activity of new neocryptolepine derivatives.
Jonckers TH, van Miert S, Cimanga K, Bailly C, Colson P, De Pauw-Gillet MC, van den Heuvel H, Claeys M, Lemière F, Esmans EL, Rozenski J, Quirijnen L, Maes L, Dommisse R, Lemière GL, Vlietinck A, Pieters L.
Jonckers TH, et al. Among authors: lemiere gl.
J Med Chem. 2002 Aug 1;45(16):3497-508. doi: 10.1021/jm011102i.
J Med Chem. 2002.
PMID: 12139461
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2-Substituted 4-, 5-, and 6-[(1E)-3-oxo-3-phenylprop-1-en-1-yl]pyridazin-3(2H)-ones and 2-substituted 4,5-bis[(1E)-3-oxo-3-phenylprop-1-en-1-yl]pyridazin-3(2H)-ones as potent platelet aggregation inhibitors: design, synthesis, and SAR studies.
Meyers C, Yáñez M, Elmaatougi A, Verhelst T, Coelho A, Fraiz N, Lemière GL, García-Mera X, Laguna R, Cano E, Maes BU, Sotelo E.
Meyers C, et al. Among authors: lemiere gl.
Bioorg Med Chem Lett. 2008 Jan 15;18(2):793-7. doi: 10.1016/j.bmcl.2007.11.034. Epub 2007 Nov 17.
Bioorg Med Chem Lett. 2008.
PMID: 18053717
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Pyridazines part 41: synthesis, antiplatelet activity and SAR of 2,4,6-substituted 5-(3-oxo-3-phenylprop-1-en-1-yl)- or 5-(3-phenylprop-2-enoyl)pyridazin-3(2H)-ones.
Crespo A, Meyers C, Coelho A, Yáñez M, Fraiz N, Sotelo E, Maes BU, Laguna R, Cano E, Lemière GL, Raviña E.
Crespo A, et al. Among authors: lemiere gl.
Bioorg Med Chem Lett. 2006 Feb 15;16(4):1080-3. doi: 10.1016/j.bmcl.2005.10.073. Epub 2005 Nov 14.
Bioorg Med Chem Lett. 2006.
PMID: 16290144
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The first tandem double palladium-catalyzed aminations: synthesis of dipyrido[1,2-a:3',2'-d]imidazole and its benzo- and aza-analogues.
Loones KT, Maes BU, Dommisse RA, Lemière GL.
Loones KT, et al. Among authors: lemiere gl.
Chem Commun (Camb). 2004 Nov 7;(21):2466-7. doi: 10.1039/b409161b. Epub 2004 Sep 20.
Chem Commun (Camb). 2004.
PMID: 15514818
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