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The H274Y mutation in the influenza A/H1N1 neuraminidase active site following oseltamivir phosphate treatment leave virus severely compromised both in vitro and in vivo

Antiviral research, 2002-08, Vol.55 (2), p.307-317

2002

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Novel Benzisoxazole Derivatives as Potent and Selective Inhibitors of Acetylcholinesterase

Journal of medicinal chemistry, 1994-08, Vol.37 (17), p.2721-2734

1994

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3-(1,2,5,6-Tetrahydropyrid-4-yl)pyrrolo[3,2-b]pyrid-5-one: a potent and selective serotonin (5-HT1) agonist and rotationally restricted phenolic analog of 5-methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl)indole

Journal of medicinal chemistry, 1990-08, Vol.33 (8), p.2087-2093

1990

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Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors

Journal of medicinal chemistry, 1995-03, Vol.38 (7), p.1084-1089

1995

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Thiazole as a carbonyl bioisostere. A novel class of highly potent and selective 5-HT3 receptor antagonists

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2715-2720

1990

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La transcendantalité du langage

Archives de philosophie, 2020, Vol.83 (1), p.39-48

2020

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5,7-dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H- pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: a potent and centrally-selective inhibitor of acetylcholinesterase with an improved margin of safety

Journal of medicinal chemistry, 1995-07, Vol.38 (15), p.2802

1995

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A novel method for converting ketones to .alpha.-diketones. The reaction of enamino ketones with singlet oxygen

Journal of the American Chemical Society, 1976-11, Vol.98 (24), p.7868-7869

1976

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Reaction of singlet oxygen with enamino carbonyl systems. A general method for the synthesis of .alpha.-keto derivatives of lactones, esters, amides, lactams, and ketones

Journal of organic chemistry, 1985-09, Vol.50 (19), p.3573-3580

1985

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Calcium-independent phosphodiesterase inhibitors as putative antidepressants : [3-(bicycloakyloxy)-4-methoxyphenyl]-2-imidazolidinones

Journal of medicinal chemistry, 1991, Vol.34 (1), p.291-298

1991

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Synthesis, in vitro binding profile, and central nervous system penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl5-(4)-imidazolylmethyl]thiazole

Journal of medicinal chemistry, 1990-11, Vol.33 (11), p.3020-3023

1990

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Developmental status of synthetic immunomodulators

The Year in immunology, 1985, p.193

1985

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Robert Marteau, arpenteur en vers et proses

2015

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Singlet oxygen in organic synthesis

Tetrahedron, 1981, Vol.37 (10), p.1825-1852

1981

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5,7-Dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]ethyl]-6H-pyrrolo[3,2-f]-1,2-benzisoxazol-6-one : a potent and centrally-selective inhibitor of acetylcholinesterase with an improved margin of safety

Journal of medicinal chemistry, 1995, Vol.38 (15), p.2802-2808

1995

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Synthesis, in vitro binding profile, and central nervous system penetrability of the highly potent 5-HT sub(3) receptor antagonist ( super(3)H)-4-(2-methoxyphenyl)-2-(4(5)-methyl-5(4)-imidazolylmethy l)-thiazole

Journal of medicinal chemistry, 1990-01, Vol.33 (11), p.3020-3023

1990

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Reaction of singlet oxygen with enamino lactones. Conversion of lactones to .alpha.-keto lactones

Journal of organic chemistry, 1978-08, Vol.43 (16), p.3238-3240

1978

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Analysis of torsional spectra of molecules with two internal C3ν, rotors—XXVI. A far infrared study of 1,1-dimethylhydrazine

Spectrochimica acta. Part A: Molecular spectroscopy, 1994, Vol.50 (3), p.521-538

1994

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Analysis of torsional spectra of molecules with two internal C3v, rotors :. XXVI: A far infrared study of 1,1-dimethylhydrazine: Spectroscopy in South Carolina. II

Spectrochimica acta. Part A: Molecular spectroscopy, 1994, Vol.50 (3), p.521-538

1994

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ChemInform Abstract: 5,7-Dihydro-3-(2-(1-(phenylmethyl)-4-piperidinyl)ethyl)-6H-pyrrolo(3,2- f)-1,2-benzisoxazol-6-one: A Potent and Centrally-Selective Inhibitor of Acetylcholinesterase with an Improved Margin of Safety

ChemInform, 1995-11, Vol.26 (48), p.no-no

1995

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ChemInform Abstract: Thiazole as a Carbonyl Bioisostere. A Novel Class of Highly Potent and Selective 5-HT3 Receptor Antagonists

ChemInform, 1991-03, Vol.22 (10), p.no-no

1991

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ChemInform Abstract: 3-(1,2,5,6-Tetrahydropyrid-4-yl)pyrrolo(3,2-b)pyrid-5-one: A Potent and Selective Serotonin (5-HT1B) Agonist and Rotationally Restricted Phenolic Analogue of 5-Methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl)indole

ChemInform, 1991-01, Vol.22 (4), p.no-no

1991

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The Reductive Decyanation of Nitriles by Alkali Fusion

Synthetic communications, 1980-01, Vol.10 (12), p.939-945

1980

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ChemInform Abstract: Calcium-Independent Phosphodiesterase Inhibitors as Putative Antidepressants: (3-(Bicycloalkoxy)-4-methoxyphenyl)-2- imidazolidinones

ChemInform, 1991-06, Vol.22 (24), p.no-no

1991

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Dopamine agonist therapy in early Parkinson's disease

Cochrane database of systematic reviews, 2008-01 (2), p.CD006564

2008

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