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Potent, non-thiol inhibitors of farnesyltransferase

Bioorganic & medicinal chemistry letters, 1998-12, Vol.8 (23), p.3311-3316

1998

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Synthesis of one of the major mouse metabolites of lovastatin and simvastatin

Bioorganic & medicinal chemistry letters, 1993-12, Vol.3 (12), p.2755-2758

Stokker, G.E.

1993

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

Tetrahedron letters, 1996-07, Vol.37 (31), p.5453-5456

Stokker, G.E.

1996

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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

Journal of medicinal chemistry, 1986-02, Vol.29 (2), p.170-181

1986

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

Journal of medicinal chemistry, 1983-04, Vol.26 (4), p.580-585

1983

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

Journal of medicinal chemistry, 1985-03, Vol.28 (3), p.347-358

1985

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

Journal of organic chemistry, 1993-08, Vol.58 (18), p.5015-5016

1993

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

Journal of medicinal chemistry, 1986-05, Vol.29 (5), p.852-855

1986

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

Journal of medicinal chemistry, 1986-05, Vol.29 (5), p.825-841

1986

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Synthesis of the 3′(S)-hydroxy derivative of simvastatin

Bioorganic & medicinal chemistry letters, 1994-07, Vol.4 (14), p.1767-1770

Stokker, G.E.

1994

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Synthesis of 5,7-dichloro-2H-1-benzopyran-2-ol

Journal of heterocyclic chemistry, 1984-03, Vol.21 (2), p.609-610

Stokker, G. E.

1984

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

Tetrahedron letters, 1987, Vol.28 (28), p.3179-3182

Stokker, Gerald E

1987

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(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids

Journal of medicinal chemistry, 1984-07, Vol.27 (7), p.840-845

1984

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

Journal of medicinal chemistry, 1980-12, Vol.23 (12), p.1414-1427

1980

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Synthesis and X-ray characterization of 6(S)-epi-mevinolin, a lactone epimer

Journal of organic chemistry, 1986-12, Vol.51 (25), p.4931-4934

1986

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

Journal of medicinal chemistry, 1982-06, Vol.25 (6), p.735-742

1982

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

Journal of medicinal chemistry, 1981-09, Vol.24 (9), p.1063-1067

1981

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2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol

Journal of medicinal chemistry, 1981-01, Vol.24 (1), p.115-117

1981

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Structure of the diuretic merbaphen

Journal of medicinal chemistry, 1971-10, Vol.14 (10), p.998-999

1971

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2-(Aminomethyl)phenols, a new class of saluretic agents. 6. Effects of N,O-spiroannulation and subsequent quaternization

Journal of medicinal chemistry, 1983-04, Vol.26 (4), p.585-590

1983

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

Journal of organic chemistry, 1986-12, Vol.51 (25), p.4931-4934

1986

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3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 2. Structural modification of 7-(substituted aryl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives

Journal of medicinal chemistry, 1986-02, Vol.29 (2), p.159-169

1986

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Synthesis and characterization of a novel 6-heteroaryl-3,6-dihydro-2H-pyran-2-acetic acid

Heterocycles, 1987, Vol.26 (1), p.157-162

1987

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Synthesis of L-669,262, a Potent HMG-CoA Reductase Inhibitor

Journal of organic chemistry, 1994-10, Vol.59 (20), p.5983-5986

Stokker, Gerald E

1994

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The Use of Sterically Hindered Benzylamines in the Sommelet Reaction

Synthetic communications, 1982-01, Vol.12 (11), p.847-853

1982

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Potent, non-thiol inhibitors of farnesyltransferase

Synthesis of one of the major mouse metabolites of lovastatin and simvastatin

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

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

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

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

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

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

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

Synthesis of the 3′(S)-hydroxy derivative of simvastatin

Synthesis of 5,7-dichloro-2H-1-benzopyran-2-ol

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

(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids

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

Synthesis and X-ray characterization of 6(S)-epi-mevinolin, a lactone epimer

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

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

2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol

Structure of the diuretic merbaphen

2-(Aminomethyl)phenols, a new class of saluretic agents. 6. Effects of N,O-spiroannulation and subsequent quaternization

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

3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 2. Structural modification of 7-(substituted aryl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives

Synthesis and characterization of a novel 6-heteroaryl-3,6-dihydro-2H-pyran-2-acetic acid

Synthesis of L-669,262, a Potent HMG-CoA Reductase Inhibitor

The Use of Sterically Hindered Benzylamines in the Sommelet Reaction

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