D. Hageman

发表

Anilinoquinazoline inhibitors of fructose 1,6-bisphosphatase bind at a novel allosteric site: synthesis, in vitro characterization, and X-ray crystallography.

M. Mansour, D. Danley, G. Schulte, 2002, Journal of medicinal chemistry.

3-(2-carboxyethyl)-4,6-dichloro-1H-indole-2-carboxylic acid: an allosteric inhibitor of fructose-1,6-bisphosphatase at the AMP site.

M. Mansour, D. Danley, G. Schulte, 2003, Bioorganic & medicinal chemistry letters.

CP-70,030 and CP-75,998: The first non-peptide antagonists of bombesin and gastrin releasing peptide

D. Hageman, R. Spencer, R. Snider, 1992 .

Fluoride-Mediated Boronic Acid Coupling Reactions

S. Wright, D. Hageman, L. D. Mcclure, 1994 .

Convenient preparations of t-butyl esters and ethers from t-butanol

S. Wright, D. Hageman, L. D. Mcclure, 1997 .

Convenient Preparations of t‐Butyl Esters and Ethers from t‐Butanol.

S. Wright, D. Hageman, L. D. Mcclure, 1998 .

A convenient modification of the Gassman oxindole synthesis

S. Wright, D. Hageman, L. D. Mcclure, 1996 .

5-Phenyl-3-ureidobenzazepin-2-ones as cholecystokinin-B receptor antagonists.

D. Hageman, J. Lowe, S. Zorn, 1994, Journal of medicinal chemistry.

A synthesis of functionalized indoline 2,2-biscarboxylates

S. Wright, D. Hageman, L. D. Mcclure, 1996 .

SYNTHESIS OF FUNCTIONALIZED 3-PYRIDYL METHYL KETONES

S. Wright, D. Hageman, L. D. Mcclure, 1998 .

5-Chloroindoloyl glycine amide inhibitors of glycogen phosphorylase: synthesis, in vitro, in vivo, and X-ray crystallographic characterization.

V. L. Rath, S. Wright, D. Hageman, 2005, Bioorganic & medicinal chemistry letters.

Allosteric inhibition of fructose-1,6-bisphosphatase by anilinoquinazolines.

S. Wright, A. Carlo, D. Hageman, 2001, Bioorganic & medicinal chemistry letters.

Fluoride‐Mediated Boronic Acid Coupling Reactions.

S. Wright, D. Hageman, L. D. Mcclure, 1995 .