G. Stokker

发表

3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 1. Structural modification of 5-substituted 3,5-dihydroxypentanoic acids and their lactone derivatives.

B. E. Evans, W. F. Hoffman, A. Deana, 1985, Journal of Medicinal Chemistry.

Synthesis and x-ray characterization of 6(S)-epimevinolin, a lactone epimer

C. Rooney, G. Stokker, J. M. Wiggins, 1986 .

3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted [1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives.

W. F. Hoffman, P. Anderson, J. Hirshfield, 1986, Journal of Medicinal Chemistry.

3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 5. 6-(Fluoren-9-yl)- and 6-(fluoren-9-ylidenyl)-3,5-dihydroxyhexanoic acids and their lactone derivatives.

A. Alberts, R. Smith, J. Huff, 1986, Journal of medicinal chemistry.

2-(AMINOMETHYL)PHENOLS, A NEW CLASS OF SALURETIC AGENTS. 5. FUSED-RING ANALOGS

A. Deana, Robert L. Smith, G. Stokker, 1983 .

2-(Aminomethyl)phenols, a new class of saluretic agents. 5. Fused-ring analogues.

A. Deana, R. Smith, G. Stokker, 1983, Journal of medicinal chemistry.

2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution

A. Deana, C. Sweet, Robert L. Smith, 1981 .

Potent, non-thiol inhibitors of farnesyltransferase.

D. Pompliano, S. Graham, J. Hutchinson, 1998, Bioorganic & medicinal chemistry letters.

HMG-CoA reductase inhibitors

O. Hensens, G. Hartman, G. Stokker, 1991 .

In vitro and in vivo biotransformation of simvastatin, an inhibitor of HMG CoA reductase.

B. Arison, S. Pitzenberger, G. Stokker, 1990, Drug metabolism and disposition: the biological fate of chemicals.

2-(Aminomethyl)phenols, a new class of saluretic agents. 3. Effects of functional group reorientation and modification.

A. Deana, G. Stokker, E. Cragoe, 1981, Journal of Medicinal Chemistry.

2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.

A. Deana, C. Sweet, G. Stokker, 1980, Journal of medicinal chemistry.

Palladium catalyzed stereospecific Michael arylation of 6-alkyl-5,6-dihydro-2H-pyran-2-ones

G. Stokker, 1987 .

Preparation of 1,2-benzisoxazoles from salicylaldoximes via trichloroacetyl isocyanate

G. Stokker, 1983 .

Preparation of 1,2,3,4-tetrahydroisoquinolines lacking electron donating groups — An intramolecular cyclization complementary to the Pictet-Spengler reaction

G. Stokker, 1996 .

2-(Aminomethyl)phenols, a new class of saluretic agents. 4. Effects of oxygen and/or nitrogen substitution.

A. Deana, G. Stokker, E. Cragoe, 1982, Journal of medicinal chemistry.

2-Aminomethylphenols: A New Class of Saluretic Agents

G. Stokker, E. Cragoe, E. Schultz, 1978 .

Preparation of 1,2,3,4‐Tetrahydroisoquinolines Lacking Electron Donating Groups ‐ An Intramolecular Cyclization Complementary to the Pictet‐Spengler Reaction.

G. Stokker, 1996 .

Deoxymercuration in the Presence of Both Acid and Iodide Ion1

G. Stokker, M. M. Kreevoy, A. K. Ahmed, 1963 .

Agents for the treatment of brain edema. 2. [(2,3,9,9a-Tetrahydro-3-oxo-9a-substituted-1H-fluoren-7-yl)oxy]+ ++alkanoi c acids and some of their analogues.

P. Anderson, H. Kimelberg, G. Stokker, 1986, Journal of medicinal chemistry.

3-HYDROXY-3-METHYLGLUTARYL-COENZYME A REDUCTASE INHIBITORS. I. STRUCTURAL MODIFICATION OF 5-SUBSTITUTED 3,5-DIHYDROXYPENTANOIC ACIDS AND THEIR LACTONE DERIVATIVES

W. F. Hoffman, A. Deana, A. Alberts, 1985 .

The Use of Sterically Hindered Benzylamines in the Sommelet Reaction

G. Stokker, E. Schultz, 1983 .

2-(AMINOMETHYL)PHENOLS, A NEW CLASS OF SALURETIC AGENTS. 3. EFFECTS OF FUNCTIONAL GROUP REORIENTATION AND MODIFICATION

A. Deana, Robert L. Smith, G. Stokker, 1982 .

A simple and inexpensive synthesis of 4-(aminomethyl)-L-phenylalanine

W. F. Hoffman, G. Stokker, C. Homnick, 1993 .

Palladium Catalyzed Stereospecific Michael Arylation of 6-Alkyl-5,6-dihydro-2H-pyran-2-ones.

G. Stokker, 1987 .

Synthesis of 7-(4′-fluoro-3,3′,5-trimethyl[1,1′-biphenyl]-2-YL)-3-hydroxy-5-OXO-5-13C-heptanoic acid and trans-6-[2-(4′-fluoro −3,3′,5-trimethyl[1,1′-biphenyl]-2-YL)ethyl]-3,4,5,6-tetrahydro-6-13C-4-hydroxy-2H-pyran-2-one

G. Stokker, 1987 .

3-Hydroxy-3-methylglutaryl-coenzyme A Reductase Inhibitors. Part 3.

W. F. Hoffman, P. Anderson, J. Hirshfield, 1986 .