C. Rooney

发表

2-Pyridinone derivatives: a new class of nonnucleoside, HIV-1-specific reverse transcriptase inhibitors.

Christopher M Thomas, J. Nunberg, W. S. Saari, 1991, Journal of medicinal chemistry.

Synthesis and evaluation of 2-pyridinone derivatives as HIV-1-specific reverse transcriptase inhibitors. 2. Analogues of 3-aminopyridin-2(1H)-one.

Christopher M Thomas, W. S. Saari, J. Hoffman, 1992, Journal of medicinal chemistry.

Synthesis and evaluation of 2-pyridinone derivatives as HIV-1-specific reverse transcriptase inhibitors. 4. 3-[2-(Benzoxazol-2-yl)ethyl]-5-ethyl-6-methylpyridin-2(1H)-one and analogues.

Christopher M Thomas, J. Hoffman, J. Wai, 1993, Journal of medicinal chemistry.

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

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

Chapter 17. Progress in Atherosclerosis Therapy: Hypolipidemic Agents

C. Rooney, J. D. Prugh, 1983 .

Rational Design of a Dual-Mode Optical and Chemical Prodrug

David S. Jones, S. Gorman, C. McCoy, 2006, Pharmaceutical Research.

Quantitative structure-activity relationships involving the inhibition of glycolic acid oxidase by derivatives of glycolic and glyoxylic acids.

P. Anderson, E. Eichler, W. Randall, 1979, Journal of medicinal chemistry.

Light-triggered molecule-scale drug dosing devices.

S. Gorman, C. McCoy, C. Rooney, 2007, Journal of the American Chemical Society.

Inhibitors of glycolic acid oxidase. 4-substituted 2,4-dioxobutanoic acid derivatives.

A. Patchett, E. Eichler, W. Randall, 1983, Journal of medicinal chemistry.

Cyclic amidine inhibitors of indolamine N-methyltransferase.

N. R. Hunter, P. Anderson, J. Rokach, 1979, Journal of medicinal chemistry.

Synthesis of 2-, 3- and 9-substituted 11-oxo-11H-pyrrolo[2,1-b][3]benzazepines

C. Rooney, S. F. Britcher, P. Belanger, 1983 .

Synthesis, chemistry, and photochemical substitutions of 6,11-dihydro-5H-pyrrolo[2,1-b][3]benzazepin-11-ones

J. Rokach, Y. Girard, C. Rooney, 1983 .

1,8‐Naphthyridines. Part I. Synthesis of some trifluoromethyl‐1,8‐naphthyridine derivatives

E. Eichler, C. Rooney, H. W. Williams, 1976 .

5-chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase.

W. Greenlee, T. Ciccarone, J. Condra, 1993, Journal of medicinal chemistry.

Inhibitors of indoleethylamine N-methyltransferase. Derivatives of 3-methyl-2-thiazolidinimine. In vitro, in vivo, and metabolic studies.

J. Rokach, P. Hamel, Y. Girard, 1980, Journal of medicinal chemistry.

Synthesis and evaluation of 2-pyridinone derivatives as specific HIV-1 reverse transcriptase inhibitors. 3. Pyridyl and phenyl analogs of 3-aminopyridin-2(1H)-one.

Christopher M Thomas, W. S. Saari, J. Hoffman, 1993, Journal of medicinal chemistry.

1,8‐NAPHTHYRIDINES. PART II. SYNTHESIS OF SOME 3‐PYRIDYL‐5,7‐DI(TRIFLUOROMETHYL)‐1,8‐NAPHTHYRIDIN‐2(1H)ONES

E. Eichler, C. Rooney, H. W. Williams, 1976 .

SYNTHESIS OF SULFONYLHYDRAZINE DERIVATIVES WITH MONOAMINE OXIDASE INHIBITORY ACTIVITY.

J. Sprague, C. Rooney, E. Cragoe, 1962, Journal of medicinal and pharmaceutical chemistry.

Synthesis and utilization of the chiral synthon methyl 3-O-benzyl-2,4,6-trideoxy-6-iodo-.alpha.-D-erythro-hexopyranoside in the synthesis of a potent HMG-CoA reductase inhibitor

A. Deana, C. Rooney, J. D. Prugh, 1986 .

5‐Chloro‐3‐(phenylsulfonyl)indole‐2‐carboxamide: A Novel, Non‐ Nucleoside Inhibitor of HIV‐1 Reverse Transcriptase.

W. Greenlee, P. Anderson, T. Ciccarone, 1994 .

Nucleophilic displacement of activated aryl triflates a new synthesis of oxindoles and arylacetic acids

Y. Girard, E. Engelhardt, C. Rooney, 1979 .

Utilization of the chiral synthon, methyl 3-O-benzyl-2,4,6-trideoxy-6-iodo-α-D-erythro-hexopyranoside in the synthesis of a potent HMG-CoA reductase inhibitor

A. Deana, C. Rooney, J. D. Prugh, 1985 .

Kojic amine--a novel gamma-aminobutyric acid analogue.

J. Rokach, Y. Girard, C. Rooney, 1979, Journal of medicinal chemistry.

Inhibitors of glycolic acid oxidase. 4-Substituted 3-hydroxy-1H-pyrrole-2,5-dione derivatives.

E. Eichler, W. Randall, E. Ulm, 1983, Journal of medicinal chemistry.

SOME FLUORINE SUBSTITUTED TOLANES

C. Rooney, A. N. Bourns, 1955 .

2-(2-Oxo-1-phthalimidoethylidenyl)-1,3-dithiolane. An Unexpected Product from an Attempted Cleavage of a Dithiolane with Ceric Ammonium Nitrate

C. Rooney, H. W. Williams, 1977 .

Urinary metabolites of timolol from humans and laboratory animals. Syntheses and beta-adrenergic blocking activities.

O. Hensens, B. Arison, C. Rooney, 1980, Journal of medicinal chemistry.

URINARY METABOLITES OF TIMOLOL FROM HUMANS AND LABORATORY ANIMALS. SYNTHESES AND β-ADRENERGIC BLOCKING ACTIVITIES

O. Hensens, B. Arison, C. Rooney, 1981 .

The alpha-hydrazino analog of histidine.

C. Rooney, R. Firestone, M. Sletzinger, 1968, Journal of Medicinal Chemistry.

3,4-Dihydro-2H-1,5-benzodioxepins. A Novel Class of β-Adrenergic Stimulants

C. Rooney, R. S. Stuart, H. W. Williams, 1975 .

CHEMICAL INTERACTIONS OF AMINO COMPOUNDS AND SUGARS. VI.1 THE REPEATING UNIT IN BROWNING POLYMERS2

M. Wolfrom, C. Rooney, A. W. Langer, 1953 .

A synthesis of 6-hydroxy-1-benzoxepin-3,5(2H,4H)-dione

P. Hamel, C. Rooney, B. K. Wasson, 1977 .

Metabolism of 3-[2-(benzoxazol-2-yl)ethyl]-5-ethyl-6-methylpyridin-2 (1H)-one (L-696,229), an HIV-1 reverse transcriptase inhibitor, by rat liver slices and in humans.

T. Olah, B. Arison, S. Varga, 1994, Drug metabolism and disposition: the biological fate of chemicals.

Chemical Interactions of Amino Compounds and Sugars. VIII.1Influence of Water2

M. Wolfrom, C. Rooney, 1953 .

1,8-Naphthyridines. Part III. Synthesis of some 6-substituted-1,8-naphthyridin-2(1H)ones†

E. Eichler, C. Rooney, H. W. Williams, 1976 .

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

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

Origin of monacolin L from Aspergillus terreus cultures.

C. Rooney, R. Reamer, H. Ramjit, 1989, The Journal of antibiotics.