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Mild and General Methods for the Palladium-Catalyzed Cyanation of Aryl and Heteroaryl Chlorides

Organic letters, 2007-04, Vol.9 (9), p.1711-1714

2007

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Inhibitors of human mitotic kinesin Eg5: Characterization of the 4-phenyl-tetrahydroisoquinoline lead series

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (8), p.2095-2100

2006

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Synthesis and Biological Evaluation of 1-Aryl-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-4-one Inhibitors of Cyclin-Dependent Kinases

Journal of medicinal chemistry, 2004-11, Vol.47 (24), p.5894-5911

2004

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Identification of selective inhibitors of cyclin dependent kinase 4

Bioorganic & medicinal chemistry letters, 2001-08, Vol.11 (16), p.2209-2211

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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DPC 681 and DPC 684: Potent, Selective Inhibitors of Human Immunodeficiency Virus Protease Active against Clinically Relevant Mutant Variants

Antimicrobial Agents and Chemotherapy, 2001-11, Vol.45 (11), p.3021-3028

2001

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Preparation and Structure−Activity Relationship of Novel P1/P1‘-Substituted Cyclic Urea-Based Human Immunodeficiency Virus Type-1 Protease Inhibitors

Journal of medicinal chemistry, 1996-05, Vol.39 (11), p.2156-2169

1996

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Stereoisomers of Cyclic Urea HIV-1 Protease Inhibitors: Synthesis and Binding Affinities

Journal of medicinal chemistry, 1998-12, Vol.41 (25), p.5113-5117

1998

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Calculated and Experimental Low-Energy Conformations of Cyclic Urea HIV Protease Inhibitors

Journal of the American Chemical Society, 1998-05, Vol.120 (19), p.4570-4581

1998

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Discovery of an Oxycyclohexyl Acid Lysophosphatidic Acid Receptor 1 (LPA1) Antagonist BMS-986278 for the Treatment of Pulmonary Fibrotic Diseases

Journal of medicinal chemistry, 2021-11, Vol.64 (21), p.15549-15581

2021

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Phospholipase C Inhibitors: A New Class of Agents

Journal of medicinal chemistry, 1994-07, Vol.37 (14), p.2232-2237

1994

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Chiral synthetic macrodiolide and macrotriolide ionophores with C2- and C2symmetry

Tetrahedron letters, 1990, Vol.31 (37), p.5285-5288

1990

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Increased antiviral activity of cyclic urea HIV protease inhibitors by modifying the P1/P1′ substituents

Bioorganic & medicinal chemistry letters, 1999-08, Vol.9 (15), p.2259-2262

1999

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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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Synthesis and Biological Evaluation of 1-Aryl-4,5-dihydro-1 H -pyrazolo[3,4- d ]pyrimidin-4-one Inhibitors of Cyclin-Dependent Kinases

Journal of medicinal chemistry, 2004-11, Vol.47 (24), p.5894-5911

2004

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Clinical investigation (In Vivo) of endodontically treated maxillary first molars

Journal of endodontics, 1987-10, Vol.13 (10), p.506-512

1987

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The synthesis and antitumor evaluation of unsymmetrical bis-imides

Bioorganic & medicinal chemistry letters, 1997-01, Vol.7 (2), p.163-168

1997

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Functionalized aliphatic P2/P2′ analogs of HIV-1 protease inhibitor DMP323

Bioorganic & medicinal chemistry letters, 1997-06, Vol.7 (11), p.1365-1370

1997

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Synthesis and enzymatic properties of a deoxy analog of phosphatidylinositol

Bioorganic & medicinal chemistry letters, 1992, Vol.2 (2), p.171-174

1992

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Mild and General Methods for the Palladium-Catalyzed Cyanation of Aryl and Heteroaryl Chlorides

ChemInform, 2007-08, Vol.38 (35), p.no-no

2007

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Synthesis, Antiviral Activity and Pharmacokinetics of P1/P1′ Substituted 3-Aminoindazole Cyclic Urea HIV Protease Inhibitors

ChemInform, 2003-06, Vol.34 (24), p.no-no

2003

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Pioneer CESA Guidance Project: A Staff Development Program for School Counselors. Group Facilitation

Kaltenbach, Robert F

1977

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ChemInform Abstract: Increased Antiviral Activity of Cyclic Urea HIV Protease Inhibitors by Modifying the P1/P1′ Substituents

ChemInform, 1999-11, Vol.30 (46), p.no-no

1999

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Effect of a Hospital and Postdischarge Quality Improvement Intervention on Clinical Outcomes and Quality of Care for Patients With Heart Failure With Reduced Ejection Fraction: The CONNECT-HF Randomized Clinical Trial

JAMA : the journal of the American Medical Association, 2021-07, Vol.326 (4), p.314

2021

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Care Optimization Through Patient and Hospital Engagement Clinical Trial for Heart Failure: Rationale and design of CONNECT-HF

The American heart journal, 2020-02, Vol.220, p.41-50

2020

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Mild and General Methods for the Palladium-Catalyzed Cyanation of Aryl and Heteroaryl Chlorides

Inhibitors of human mitotic kinesin Eg5: Characterization of the 4-phenyl-tetrahydroisoquinoline lead series

Synthesis and Biological Evaluation of 1-Aryl-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-4-one Inhibitors of Cyclin-Dependent Kinases

Identification of selective inhibitors of cyclin dependent kinase 4

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

DPC 681 and DPC 684: Potent, Selective Inhibitors of Human Immunodeficiency Virus Protease Active against Clinically Relevant Mutant Variants

Preparation and Structure−Activity Relationship of Novel P1/P1‘-Substituted Cyclic Urea-Based Human Immunodeficiency Virus Type-1 Protease Inhibitors

Stereoisomers of Cyclic Urea HIV-1 Protease Inhibitors: Synthesis and Binding Affinities

Calculated and Experimental Low-Energy Conformations of Cyclic Urea HIV Protease Inhibitors

Discovery of an Oxycyclohexyl Acid Lysophosphatidic Acid Receptor 1 (LPA1) Antagonist BMS-986278 for the Treatment of Pulmonary Fibrotic Diseases

Phospholipase C Inhibitors: A New Class of Agents

Chiral synthetic macrodiolide and macrotriolide ionophores with C2- and C2symmetry

Increased antiviral activity of cyclic urea HIV protease inhibitors by modifying the P1/P1′ substituents

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

Synthesis and Biological Evaluation of 1-Aryl-4,5-dihydro-1 H -pyrazolo[3,4- d ]pyrimidin-4-one Inhibitors of Cyclin-Dependent Kinases

Clinical investigation (In Vivo) of endodontically treated maxillary first molars

The synthesis and antitumor evaluation of unsymmetrical bis-imides

Functionalized aliphatic P2/P2′ analogs of HIV-1 protease inhibitor DMP323

Synthesis and enzymatic properties of a deoxy analog of phosphatidylinositol

Mild and General Methods for the Palladium-Catalyzed Cyanation of Aryl and Heteroaryl Chlorides

Synthesis, Antiviral Activity and Pharmacokinetics of P1/P1′ Substituted 3-Aminoindazole Cyclic Urea HIV Protease Inhibitors

Pioneer CESA Guidance Project: A Staff Development Program for School Counselors. Group Facilitation

ChemInform Abstract: Increased Antiviral Activity of Cyclic Urea HIV Protease Inhibitors by Modifying the P1/P1′ Substituents

Effect of a Hospital and Postdischarge Quality Improvement Intervention on Clinical Outcomes and Quality of Care for Patients With Heart Failure With Reduced Ejection Fraction: The CONNECT-HF Randomized Clinical Trial

Care Optimization Through Patient and Hospital Engagement Clinical Trial for Heart Failure: Rationale and design of CONNECT-HF

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