Paul D. Hill

Cross-Coupling Methods for the Large-Scale Preparation of an Imidazole−Thienopyridine:  Synthesis of [2-(3-Methyl-3H-imidazol-4-yl)- thieno[3,2-<i>b</i>]pyridin-7-yl]-(2-methyl-1H-indol-5-yl)-amine

John A. Ragan, Jeffrey W. Raggon, Paul D. Hill et al. · Organic Process Research & Development · 2003 · 59 citations

Cross-coupling Methods, Organostannane Reagent, Diversity Oriented Synthesis +13

Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro-<i>s</i>-indacen-4-yl)-3-[4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Anti-inflammatory Agent

Frank J. Urban, V. John Jasys, Jeffrey W. Raggon et al. · Synthetic Communications · 2003 · 25 citations

Anti-inflammatory, Biochemistry, Ammonium Bicarbonate +7

Preparation of a Corticotropin-Releasing Factor Antagonist by Nucleophilic Aromatic Substitution and Copper-Mediated Ether Formation

Stéphane Caron, Nga M., Janice E. Sieser et al. · Organic Process Research & Development · 2009 · 22 citations

Medicinal Chemistry, Pharmaceutical Science, Bioorganic Chemistry +15

2,5-Dimethylpyrrole Protection Facilitates Copper(I)-Mediated Methoxylations of Aryl Iodides in the Presence of Anilines

John A. Ragan, Teresa W. Makowski, Michael J. Castaldi et al. · Synthesis · 1998 · 17 citations

Engineering, Aryl Iodides, Organic Chemistry +4