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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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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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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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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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Mesoionic pyrido[1,2- a ]pyrimidinones: Discovery of triflumezopyrim as a potent hopper insecticide 1

Bioorganic & medicinal chemistry letters, 2017-01, Vol.27 (1), p.16-20

2017

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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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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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Mesoionic pyrido[1,2-a]pyrimidinones: Discovery of triflumezopyrim as a potent hopper insecticide1

Bioorganic & medicinal chemistry letters, 2017-01, Vol.27 (1), p.16-20

2017

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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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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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Mesoionic pyrido[1,2-a]pyrimidinones: Discovery of triflumezopyrim as a potent hopper insecticide 1

Bioorganic & medicinal chemistry letters, 2017-01, Vol.27 (1), p.16

2017

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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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Convenient synthesis of L-proline benzyl ester

Bioorganic & medicinal chemistry letters, 1999-11, Vol.9 (21), p.3119-3122

1999

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Convenient synthesis of [formula omitted] benzyl ester

Bioorganic & medicinal chemistry letters, 1999-11, Vol.9 (21), p.3119-3122

1999

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

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

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

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

Mesoionic pyrido[1,2- a ]pyrimidinones: Discovery of triflumezopyrim as a potent hopper insecticide 1

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

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

Mesoionic pyrido[1,2-a]pyrimidinones: Discovery of triflumezopyrim as a potent hopper insecticide1

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

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

Mesoionic pyrido[1,2-a]pyrimidinones: Discovery of triflumezopyrim as a potent hopper insecticide 1

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

Convenient synthesis of L-proline benzyl ester

Convenient synthesis of [formula omitted] benzyl ester

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