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Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (22), p.4898-4906

2005

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Naphthylchalcones induce apoptosis and caspase activation in a leukemia cell line: The relationship between mitochondrial damage, oxidative stress, and cell death

Bioorganic & medicinal chemistry, 2010-11, Vol.18 (22), p.8026-8034

2010

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Studies dealing with cycloaddition and sigmatropic reactions of cyclopropenyl-substituted indenes

Journal of organic chemistry, 1991-07, Vol.56 (15), p.4747-4753

1991

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New and selective ryanodine receptor activators for insect control

Bioorganic & medicinal chemistry, 2009-06, Vol.17 (12), p.4127-4133

2009

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4-Azolylphenyl isoxazoline insecticides acting at the GABA gated chloride channel

Bioorganic & medicinal chemistry letters, 2013-05, Vol.23 (10), p.3001-3006

2013

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Discovery of cyantraniliprole, a potent and selective anthranilic diamide ryanodine receptor activator with cross-spectrum insecticidal activity

Bioorganic & medicinal chemistry letters, 2013-12, Vol.23 (23), p.6341-6345

2013

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Synthesis and evaluation of quinoxalinones as HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1729-1731

2000

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Agaricus bisporus fucogalactan: Structural characterization and pharmacological approaches

Carbohydrate polymers, 2013-01, Vol.92 (1), p.184-191

2013

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Synthesis and evaluation of novel quinolinones as HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 2001-07, Vol.11 (14), p.1943-1945

2001

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Polysaccharide glucomannan isolated from Heterodermia obscurata attenuates acute and chronic pain in mice

Carbohydrate polymers, 2013-02, Vol.92 (2), p.2058-2064

2013

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Discovery, synthesis, and evaluation of N-substituted amino-2(5H)-oxazolones as novel insecticides activating nicotinic acetylcholine receptors

Bioorganic & medicinal chemistry letters, 2014-05, Vol.24 (9), p.2188-2192

2014

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Synthesis and Evaluation of Efavirenz (Sustiva TM) Analogues as HIV-1 Reverse Transcriptase Inhibitors: Replacement of the Cyclopropylacetylene Side Chain

Bioorganic & medicinal chemistry letters, 2001-05, Vol.11 (9), p.1177-1179

2001

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Proline-catalyzed asymmetric assembly reactions: enzyme-like assembly of carbohydrates and polyketides from three aldehyde substrates

Tetrahedron letters, 2002-12, Vol.43 (52), p.9591-9595

2002

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Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: Novel biaryl indazoles as P2/P2′ substituents

Bioorganic & medicinal chemistry letters, 1999-11, Vol.9 (22), p.3217-3220

1999

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Novel 2,2-dioxide-4,4-disubstituted-1,3-H-2,1,3-benzothiadiazines as non-nucleoside reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 2000-01, Vol.10 (2), p.193-195

2000

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4,1-Benzoxazepinone analogues of efavirenz (Sustiva™) as HIV-1 reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 2001-06, Vol.11 (11), p.1389-1392

2001

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Synthesis, antiviral activity and pharmacokinetics of P1/P1′ substituted 3-aminoindazole cyclic urea HIV protease inhibitors

Bioorganic & medicinal chemistry letters, 2003-02, Vol.13 (4), p.605-608

2003

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A Highly Chemo- and Stereoselective Synthesis of β-Keto Esters via a Polymer-Supported Lipase Catalyzed Transesterfication

Journal of organic chemistry, 2001-03, Vol.66 (5), p.1906-1909

2001

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Trifluoromethyl-containing 3-alkoxymethyl- and 3-aryloxymethyl-2-pyridinones are potent inhibitors of HIV-1 non-nucleoside reverse transcriptase

Bioorganic & medicinal chemistry letters, 2001-02, Vol.11 (3), p.309-312

2001

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Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor Efavirenz

Bioorganic & medicinal chemistry letters, 2001-03, Vol.11 (5), p.619-622

2001

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Potent cyclic urea HIV protease inhibitors with 3-aminoindazole P2/P2′ groups

Bioorganic & medicinal chemistry letters, 1998-04, Vol.8 (7), p.715-720

1998

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3,3a-Dihydropyrano[4,3,2-de]quinazolin-2(1H)-ones are potent non-nucleoside reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.211-214

2001

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A Sequential Application of Kinetic Resolution and Polymer-Supported Scavenging for the Isolation of Chiral Secondary Alcohols

Journal of organic chemistry, 2001-08, Vol.66 (16), p.5645-5648

2001

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Potent cyclic urea HIV protease inhibitors with benzofused heterocycles as P2/P2′ groups

Bioorganic & medicinal chemistry letters, 1996-12, Vol.6 (24), p.2919-2924

1996

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The synthesis of symmetrical and unsymmetrical P1/P1′ cyclic ureas as HIV protease inhibitors

Bioorganic & medicinal chemistry letters, 1998-05, Vol.8 (9), p.1077-1082

1998

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Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators

Naphthylchalcones induce apoptosis and caspase activation in a leukemia cell line: The relationship between mitochondrial damage, oxidative stress, and cell death

Studies dealing with cycloaddition and sigmatropic reactions of cyclopropenyl-substituted indenes

New and selective ryanodine receptor activators for insect control

4-Azolylphenyl isoxazoline insecticides acting at the GABA gated chloride channel

Discovery of cyantraniliprole, a potent and selective anthranilic diamide ryanodine receptor activator with cross-spectrum insecticidal activity

Synthesis and evaluation of quinoxalinones as HIV-1 reverse transcriptase inhibitors

Agaricus bisporus fucogalactan: Structural characterization and pharmacological approaches

Synthesis and evaluation of novel quinolinones as HIV-1 reverse transcriptase inhibitors

Polysaccharide glucomannan isolated from Heterodermia obscurata attenuates acute and chronic pain in mice

Discovery, synthesis, and evaluation of N-substituted amino-2(5H)-oxazolones as novel insecticides activating nicotinic acetylcholine receptors

Synthesis and Evaluation of Efavirenz (Sustiva TM) Analogues as HIV-1 Reverse Transcriptase Inhibitors: Replacement of the Cyclopropylacetylene Side Chain

Proline-catalyzed asymmetric assembly reactions: enzyme-like assembly of carbohydrates and polyketides from three aldehyde substrates

Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: Novel biaryl indazoles as P2/P2′ substituents

Novel 2,2-dioxide-4,4-disubstituted-1,3-H-2,1,3-benzothiadiazines as non-nucleoside reverse transcriptase inhibitors

4,1-Benzoxazepinone analogues of efavirenz (Sustiva™) as HIV-1 reverse transcriptase inhibitors

Synthesis, antiviral activity and pharmacokinetics of P1/P1′ substituted 3-aminoindazole cyclic urea HIV protease inhibitors

A Highly Chemo- and Stereoselective Synthesis of β-Keto Esters via a Polymer-Supported Lipase Catalyzed Transesterfication

Trifluoromethyl-containing 3-alkoxymethyl- and 3-aryloxymethyl-2-pyridinones are potent inhibitors of HIV-1 non-nucleoside reverse transcriptase

Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor Efavirenz

Potent cyclic urea HIV protease inhibitors with 3-aminoindazole P2/P2′ groups

3,3a-Dihydropyrano[4,3,2-de]quinazolin-2(1H)-ones are potent non-nucleoside reverse transcriptase inhibitors

A Sequential Application of Kinetic Resolution and Polymer-Supported Scavenging for the Isolation of Chiral Secondary Alcohols

Potent cyclic urea HIV protease inhibitors with benzofused heterocycles as P2/P2′ groups

The synthesis of symmetrical and unsymmetrical P1/P1′ cyclic ureas as HIV protease inhibitors

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