Louis Matty | Researchain

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Featured researches published by Louis Matty.

Tetrahedron Letters | 2000

Stereoselective hydrogen bromide-promoted hydrogenation of an α-hydroxyoxime

Ian W. Davies; Mark Taylor; Jean-Francois Marcoux; Louis Matty; Jimmy Wu; David L. Hughes; Paul J. Reider

Abstract Hydrogen bromide has been demonstrated to provide optimal cis -selectivity in the reduction of 4-chromanone α-hydroxyoxime (25:1 cis / trans ) in 94% yield. This reaction is pivotal in the synthesis of cis -aminochromanol.

Journal of the American Chemical Society | 2001

Are heterogeneous catalysts precursors to homogeneous catalysts

Ian W. Davies; Louis Matty; David L. Hughes; Paul J. Reider

Journal of Organic Chemistry | 2004

Stereoselective Synthesis of a Potent Thrombin Inhibitor by a Novel P2−P3 Lactone Ring Opening†

Todd D. Nelson; Carl LeBlond; Doug E. Frantz; Louis Matty; Jeffrey V. Mitten; Damian G. Weaver; Jeffrey C. Moore; Jaehon Kim; Russell Boyd; Pei Yi Kim; Kodzo Gbewonyo; Mark Brower; Michael G. Sturr; Kathleen McLaughlin; Daniel R. McMasters; Michael H. Kress; James M. McNamara; Ulf H. Dolling

Journal of Organic Chemistry | 2005

A concise synthesis of a novel antiangiogenic tyrosine kinase inhibitor.

Joseph F. Payack; Enrique Vazquez; Louis Matty; Michael H. Kress; James M. McNamara

Journal of Organic Chemistry | 2005

An Efficient Synthesis of a Dual PPAR α/γ Agonist and the Formation of a Sterically Congested α-Aryloxyisobutyric Acid via a Bargellini Reaction

Raymond Cvetovich; John Chung; Michael H. Kress; Joseph S. Amato; Louis Matty; M. David Weingarten; Fuh-Rong Tsay; Zhen Li; George Zhou

Organic Letters | 2005

Synthesis of a Potent hNK-1 Receptor Antagonist via an SN2 Reaction of an Enantiomerically Pure α-Alkoxy Sulfonate

Todd D. Nelson; Jonathan Rosen; Jacqueline H. Smitrovich; Joseph F. Payack; Bridgette Craig; Louis Matty; Mark A. Huffman; James M. McNamara

Archive | 2005

Process for {3-[2(R)-[(1R)-1-[3,5-Bis (Trifluoromethyl) Phenyl]Ethoxy]-3(S)-(4-Fluorophenyl) Morpholin-4-Yl}-5-Oxo-4,5-Dihydro-[1,2,4]-Triazol-1-Yl}Phosphonic Acid

James M. McNamara; Louis Matty; Jonathan Rosen

Tetrahedron | 2004

An efficient synthesis of a highly functionalized 4-arylpiperidine

Genevieve N. Boice; Cecile G. Savarin; Jerry A. Murry; Karen M. Conrad; Louis Matty; Edward G. Corley; Jacqueline H. Smitrovich; Dave Hughes

Canadian Journal of Chemistry | 2002

Efficient synthesis of the optically active dihydropyrimidinone of a potent α1A- selective adrenoceptor antagonist

Daniel R. Sidler; Nancy Sue Barta; Wenjie Li; Essa Hu; Louis Matty; Nori Ikemoto; Jeffrey S Campbell; Michel Chartrain; Kozo Gbewonyo; Russell J. Boyd; Edward G. Corley; Richard G. Ball; Robert D. Larsen; Paul J. Reider

Archive | 2010