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Synthesis and Structure−Activity Relationship of Novel 6-Aryl-1,4- dihydrobenzo[d][1,3]oxazine-2-thiones as Progesterone Receptor Modulators Leading to the Potent and Selective Nonsteroidal Progesterone Receptor Agonist Tanaproget

Journal of medicinal chemistry, 2005-08, Vol.48 (16), p.5092-5095

2005

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SAR studies of 6-(arylamino)-4,4-disubstituted-1-methyl-1,4-dihydro-benzo[ d][1,3]oxazin-2-ones as progesterone receptor antagonists

Bioorganic & medicinal chemistry letters, 2007, Vol.17 (1), p.189-192

2007

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Novel 6-aryl-1,4-dihydrobenzo[ d] [1,3]oxazine-2-thiones as potent, selective, and orally active nonsteroidal progesterone receptor agonists

Bioorganic & medicinal chemistry letters, 2003-04, Vol.13 (7), p.1313-1316

2003

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Synthesis and progesterone receptor antagonist activities of 6-aryl benzimidazolones and benzothiazolones

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (20), p.2747-2750

2001

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1- or 3-(3-Amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones: Potent, Selective, and Orally Efficacious Norepinephrine Reuptake Inhibitors

Journal of medicinal chemistry, 2009-09, Vol.52 (18), p.5703-5711

2009

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6-Aryl-1,4-dihydro-benzo[d][1,3]oxazin- 2-ones: A Novel Class of Potent, Selective, and Orally Active Nonsteroidal Progesterone Receptor Antagonists

Journal of medicinal chemistry, 2002-09, Vol.45 (20), p.4379-4382

2002

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Potent nonsteroidal progesterone receptor agonists: Synthesis and SAR study of 6-aryl benzoxazines

Bioorganic & medicinal chemistry letters, 2002-03, Vol.12 (5), p.787-790

2002

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Discovery of Novel Selective Norepinephrine Inhibitors: 1-(2-Morpholin-2-ylethyl)-3-aryl-1,3-dihydro-2,1,3-benzothiadiazole 2,2-Dioxides (WYE-114152)

Journal of medicinal chemistry, 2011-10, Vol.54 (19), p.6824-6831

2011

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SAR studies of 6-aryl-1,3-dihydrobenzimidazol-2-ones as progesterone receptor antagonists

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (15), p.3600-3603

2005

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Synthesis and activity of novel 1-or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (23), p.6067-6070

2008

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3-(Arylamino)-3-phenylpropan-2-olamines as a new series of dual norepinephrine and serotonin reuptake inhibitors

Bioorganic & medicinal chemistry letters, 2009-05, Vol.19 (9), p.2464-2467

2009

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7-Aryl 1,5-dihydro-benzo[ e][1,4]oxazepin-2-ones and analogs as non-steroidal progesterone receptor antagonists

Bioorganic & medicinal chemistry, 2008-07, Vol.16 (13), p.6589-6600

2008

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Structure–activity relationships of the 1-amino-3-(1 H-indol-1-yl)-3-phenylpropan-2-ol series of monoamine reuptake inhibitors

Bioorganic & medicinal chemistry letters, 2009-10, Vol.19 (19), p.5807-5810

2009

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1,5-Dihydro-benzo[ e][1,4]oxazepin-2( 1H)-ones containing a 7-(5′-cyanopyrrol-2-yl) group as nonsteroidal progesterone receptor modulators

Bioorganic & medicinal chemistry, 2008-09, Vol.18 (18), p.5015-5017

2008

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The reaction of o-amino aryl carboxylic acids with Grignard reagents. The unusual effect of the N-protecting group on aryl ketone formation

Tetrahedron letters, 2001-03, Vol.42 (11), p.2097-2099

2001

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1- or 3-(3-Amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2 H -benzimidazol-2-ones: Potent, Selective, and Orally Efficacious Norepinephrine Reuptake Inhibitors

Journal of medicinal chemistry, 2009-09, Vol.52 (18), p.5703-5711

2009

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ChemInform Abstract: The Reaction of o-Amino Aryl Carboxylic Acids with Grignard Reagents. The Unusual Effect of the N-Protecting Group on Aryl Ketone Formation

ChemInform, 2001-06, Vol.32 (24), p.no-no

2001

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ChemInform Abstract: Potent Nonsteroidal Progesterone Receptor Agonists: Synthesis and SAR Study of 6-Aryl Benzoxazines

ChemInform, 2002-07, Vol.33 (26), p.no-no

2002

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ChemInform Abstract: Synthesis and Progesterone Receptor Antagonist Activities of 6-Aryl Benzimidazolones and Benzothiazolones

ChemInform, 2002-01, Vol.33 (4), p.no-no

2002

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Structure-property relationships that influence platinum stability in all-silica or highly siliceous zeolites

Microporous and mesoporous materials, 2023-08, Vol.358, p.112655, Article 112655

2023

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Structure-property relationships that influence platinum stability in all-silica or highly siliceous zeolites

Microporous and mesoporous materials, 2023-02, Vol.350, p.112411, Article 112411

2023

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Small Pore Aluminosilicate EMM-37: Synthesis and Structure Determination Using Continuous Rotation Electron Diffraction

Inorganic chemistry, 2019-10, Vol.58 (19), p.12854-12858

2019

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1-Methyl-1H-pyrrole-2-carbonitrile containing tetrahydronaphthalene derivatives as non-steroidal progesterone receptor antagonists

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (16), p.4816-4818

2010

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Thiourea inhibitors of herpes viruses. Part 2: N-Benzyl- N′-arylthiourea inhibitors of CMV

Bioorganic & medicinal chemistry letters, 2004-07, Vol.14 (13), p.3401-3406

2004

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Thiourea inhibitors of herpes viruses. part 1: bis-(aryl)thiourea inhibitors of CMV

Bioorganic & medicinal chemistry letters, 2003-09, Vol.13 (17), p.2929-2932

2003

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Synthesis and Structure−Activity Relationship of Novel 6-Aryl-1,4- dihydrobenzo[d][1,3]oxazine-2-thiones as Progesterone Receptor Modulators Leading to the Potent and Selective Nonsteroidal Progesterone Receptor Agonist Tanaproget

SAR studies of 6-(arylamino)-4,4-disubstituted-1-methyl-1,4-dihydro-benzo[ d][1,3]oxazin-2-ones as progesterone receptor antagonists

Novel 6-aryl-1,4-dihydrobenzo[ d] [1,3]oxazine-2-thiones as potent, selective, and orally active nonsteroidal progesterone receptor agonists

Synthesis and progesterone receptor antagonist activities of 6-aryl benzimidazolones and benzothiazolones

1- or 3-(3-Amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones: Potent, Selective, and Orally Efficacious Norepinephrine Reuptake Inhibitors

6-Aryl-1,4-dihydro-benzo[d][1,3]oxazin- 2-ones: A Novel Class of Potent, Selective, and Orally Active Nonsteroidal Progesterone Receptor Antagonists

Potent nonsteroidal progesterone receptor agonists: Synthesis and SAR study of 6-aryl benzoxazines

Discovery of Novel Selective Norepinephrine Inhibitors: 1-(2-Morpholin-2-ylethyl)-3-aryl-1,3-dihydro-2,1,3-benzothiadiazole 2,2-Dioxides (WYE-114152)

SAR studies of 6-aryl-1,3-dihydrobenzimidazol-2-ones as progesterone receptor antagonists

Synthesis and activity of novel 1-or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors

3-(Arylamino)-3-phenylpropan-2-olamines as a new series of dual norepinephrine and serotonin reuptake inhibitors

7-Aryl 1,5-dihydro-benzo[ e][1,4]oxazepin-2-ones and analogs as non-steroidal progesterone receptor antagonists

Structure–activity relationships of the 1-amino-3-(1 H-indol-1-yl)-3-phenylpropan-2-ol series of monoamine reuptake inhibitors

1,5-Dihydro-benzo[ e][1,4]oxazepin-2( 1H)-ones containing a 7-(5′-cyanopyrrol-2-yl) group as nonsteroidal progesterone receptor modulators

The reaction of o-amino aryl carboxylic acids with Grignard reagents. The unusual effect of the N-protecting group on aryl ketone formation

1- or 3-(3-Amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2 H -benzimidazol-2-ones: Potent, Selective, and Orally Efficacious Norepinephrine Reuptake Inhibitors

ChemInform Abstract: The Reaction of o-Amino Aryl Carboxylic Acids with Grignard Reagents. The Unusual Effect of the N-Protecting Group on Aryl Ketone Formation

ChemInform Abstract: Potent Nonsteroidal Progesterone Receptor Agonists: Synthesis and SAR Study of 6-Aryl Benzoxazines

ChemInform Abstract: Synthesis and Progesterone Receptor Antagonist Activities of 6-Aryl Benzimidazolones and Benzothiazolones

Structure-property relationships that influence platinum stability in all-silica or highly siliceous zeolites

Structure-property relationships that influence platinum stability in all-silica or highly siliceous zeolites

Small Pore Aluminosilicate EMM-37: Synthesis and Structure Determination Using Continuous Rotation Electron Diffraction

1-Methyl-1H-pyrrole-2-carbonitrile containing tetrahydronaphthalene derivatives as non-steroidal progesterone receptor antagonists

Thiourea inhibitors of herpes viruses. Part 2: N-Benzyl- N′-arylthiourea inhibitors of CMV

Thiourea inhibitors of herpes viruses. part 1: bis-(aryl)thiourea inhibitors of CMV

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