J. Napier

发表

Preclinical profile of remacemide: A novel anticonvulsant effective against maximal electroshock seizures in mice

J. Ordy, H. White, E. A. Swinyard, 1990, Epilepsy Research.

Discovery and Development of Metal-Catalyzed Coupling Reactions in the Synthesis of Dasabuvir, an HCV-Polymerase Inhibitor.

J. C. Marek, Brian J. Kotecki, S. Shekhar, 2019, The Journal of organic chemistry.

Synthetic applications of heteroatom-directed photoarylation. Benzo[b]furan ring construction

J. Napier, R. Ravichandran, A. Schultz, 1983 .

Studies directed at a synthesis of the morphine alkaloids. A photochemical approach

H. Kinoshita, J. Napier, R. Ravichandran, 1985 .

An enantioselective and highly convergent synthesis of (+)-ikarugamycin

R. K. Boeckman, R. Perni, J. Napier, 1989 .

Stereocontrol in the intramolecular Diels-Alder reaction. 5. Preparation of a tetracyclic intermediate for ikarugamycin

R. K. Boeckman, J. Napier, E. Thomas, 1983 .

THE NITROGEN HYPERFINE SPLITTING CONSTANT OF THE NITROXIDE FUNCTIONAL GROUP AS A SOLVENT POLARITY PARAMETER. THE RELATIVE IMPORTANCE FOR A SOLVENT POLARITY PARAMETER OF ITS BEING A CYBOTACTIC PROBE VS. ITS BEING A MODEL PROCESS

J. Napier, Bruce R. Knauer, 1976 .

THE NITROGEN HYPERFINE SPLITTING CONSTANT OF THE NITROXIDE FUNCTIONAL GROUP AS A SOLVENT POLARITY PARAMETER. THE RELATIVE IMPORTANCE FOR A SOLVENT POLARITY PARAMETER OF ITS BEING A CYBOTACTIC PROBE VS. ITS BEING A MODEL PROCESS

J. Napier, Bruce R. Knauer, 1976 .

Use of a Polymer Additive To Enhance Impurity Rejection in the Crystallization of a Pharmaceutical Compound

Venkateswarlu Bhamidi, A. Czyzewski, J. Napier, 2017 .

Concept and synthetic approach for a kilogram scale synthesis of octa-d-arginine amide nonahydrochloride salt

V. Kishore, J. Tolle, J. Napier, 2005 .

Biological profile of the metabolites and potential metabolites of the anticonvulsant remacemide

R. Griffith, M. L. Stagnitto, G. C. Palmer, 1992, Epilepsy Research.

A process for the synthesis of β-ketoesters using in-situ generated (trimethylsilyl)malonates

Xui-hong Wang, J. Napier, A. Ghannam, 1994 .

Optimization of chromone-2-carboxamide melanin concentrating hormone receptor 1 antagonists: assessment of potency, efficacy, and cardiovascular safety.

G. Diaz, E. Bush, H. Sham, 2006, Journal of medicinal chemistry.

ON THE STEREOSELECTIVITY OF HETEROATOM DIRECTED PHOTOARYLATION

J. Napier, A. Schultz, 1983 .

(-)-Spiro[1-azabicyclo[2.2.2]octane-3,5'-oxazolidin-2'-one], a conformationally restricted analogue of acetylcholine, is a highly selective full agonist at the alpha 7 nicotinic acetylcholine receptor.

J. Macor, P. Verhoest, Yanyi Zhu, 2000, Journal of medicinal chemistry.

Synthesis and evaluation of urea-based indazoles as melanin-concentrating hormone receptor 1 antagonists for the treatment of obesity.

Robin Shapiro, Ju Gao, A. Souers, 2005, Bioorganic & medicinal chemistry letters.

Preclinical profile of the anticonvulsant remacemide and its enantiomers in the rat

E. Harris, L. Freedman, H. White, 1991, Epilepsy Research.

octane-3 , 5 ′-oxazolidin-2 ′-one ] , a Conformationally Restricted Analogue of Acetylcholine , Is a Highly Selective Full Agonist at the r 7 Nicotinic Acetylcholine Receptor

J. Macor, P. Verhoest, Yanyi Zhu, 2022 .

Constrained 7-fluorocarboxychromone-4-aminopiperidine based Melanin-concentrating hormone receptor 1 antagonists: the effects of chirality on substituted indan-1-ylamines.

A. Souers, G. Diaz, E. Bush, 2007, Bioorganic & medicinal chemistry letters.

Screening for cardiovascular safety: a structure-activity approach for guiding lead selection of melanin concentrating hormone receptor 1 antagonists.

Ju Gao, Anil Vasudevan, John K Lynch, 2006, Journal of medicinal chemistry.