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Macrofilaricidal Benzimidazole–Benzoxaborole Hybrids as an Approach to the Treatment of River Blindness: Part 1. Amide Linked Analogs

ACS infectious diseases, 2020-02, Vol.6 (2), p.173-179

2020

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Macrofilaricidal Benzimidazole–Benzoxaborole Hybrids as an Approach to the Treatment of River Blindness: Part 2. Ketone Linked Analogs

ACS infectious diseases, 2020-02, Vol.6 (2), p.180-185

2020

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ChemInform Abstract: Novel Synthesis of Isoxazoline Indolizine Amides for Potential Application to Tropical Diseases

ChemInform, 2014-08, Vol.45 (33), p.no-no

2014

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ChemInform Abstract: Recent Progress in the Synthesis of Antimalarial Agents

ChemInform, 2013-03, Vol.44 (12), p.no-no

2013

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CHAPTER 7 - Linear and Macrocyclic Hepatitis C Virus Protease Inhibitors: Inhibitor Design and Macrocyclization Strategies for HCV Protease and Related Targets

Macrocycles in drug discovery, 2015, p.235-282

2015

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Annual Reports in Medicinal Chemistry: Elsevier Science Inc [distributor]

1999

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Annual Reports in Medicinal Chemistry.: Elsevier Science Inc [distributor]

1996

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Annual Reports in Medicinal Chemistry

1, 1998

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Annual Reports in Medicinal Chemistry

1, 1996

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Annual Reports in Medicinal Chemistry

1, 1997

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Annual Reports in Medicinal Chemistry

1, 1994

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Annual Reports in Medicinal Chemistry

1, 1999

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Facile synthesis of potent HIV-1 protease inhibitors containing a novel pseudo-symmetric dipeptide isostere

Journal of the Chemical Society. Chemical communications, 1993 (13), p.1052-1053

1993

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Synthesis of (±)-cycloprop-G, the cyclopropyl analogue of the broad spectrum antiviral agent cyclobut-G

Journal of the Chemical Society. Chemical communications, 1992 (2), p.128-129

1992

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Synthesis of (2S,5S,4R)-2,5-diamino-3,3-difluoro-1,6-diphenylhydroxyhexane : the core unit of a potent HIV proteinase inhibitor

Journal of the Chemical Society. Chemical communications, 1991 (2), p.110-112

1991

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Linear and Macrocyclic Hepatitis C Virus Protease Inhibitors: Inhibitor Design and Macrocyclization Strategies for HCV Protease and Related Targets

Macrocycles in Drug Discovery, 2014

Levin, Jeremy

2014

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Profile of the Renin Inhibitor, Enalkiren (ABBOTT‐64662)

Cardiovascular drug reviews, 1990-09, Vol.8 (3), p.203-219

1990

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ChemInform Abstract: Discovery and Structure-Activity Study of a Novel Benzoxaborole Antiinflammatory Agent (AN2728) for the Potential Topical Treatment of Psoriasis and Atopic Dermatitis

ChemInform, 2009-09, Vol.40 (36), p.no-no

2009

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Novel Lopinavir Analogues Incorporating Heterocyclic Replacements of Six-Member Cyclic Urea. Synthesis and Structure-Activity Relationships

ChemInform, 2004-09, Vol.35 (38), p.no-no

2004

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ChemInform Abstract: Motilides and Motilactides: Design and Development of Motilin Receptor Agonists as a New Class of Gastrointestinal Prokinetic Drugs

ChemInform, 1999-05, Vol.30 (20), p.no-no

1999

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Novel Lopinavir Analogues Incorporating Non-aromatic P-1 Side Chains - Synthesis and Structure-Activity Relationships

ChemInform, 2003-02, Vol.34 (8), p.no-no

2003

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ChemInform Abstract: Synthesis and Structure-Activity Relationships of a Novel Series of HIV-1 Protease Inhibitors Encompassing ABT-378 (Lopinavir)

ChemInform, 2002-08, Vol.33 (33), p.no-no

2002

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Chapter 7 Antihypertensive Agents

Annual Reports in Medicinal Chemistry, 1987, Vol.22, p.63-72

1987

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Synthesis and Activities of the Phosphonate Isostere of the Monophosphate of (±)Cyclobut-G

Nucleosides & nucleotides, 1992-08, Vol.11 (7), p.1383-1391

1992

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SECTION III: CANCER AND INFECTIOUS DISEASES

Annual Reports in Medicinal Chemistry, 1999, Vol.34

1999

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Macrofilaricidal Benzimidazole–Benzoxaborole Hybrids as an Approach to the Treatment of River Blindness: Part 1. Amide Linked Analogs

Macrofilaricidal Benzimidazole–Benzoxaborole Hybrids as an Approach to the Treatment of River Blindness: Part 2. Ketone Linked Analogs

ChemInform Abstract: Novel Synthesis of Isoxazoline Indolizine Amides for Potential Application to Tropical Diseases

ChemInform Abstract: Recent Progress in the Synthesis of Antimalarial Agents

CHAPTER 7 - Linear and Macrocyclic Hepatitis C Virus Protease Inhibitors: Inhibitor Design and Macrocyclization Strategies for HCV Protease and Related Targets

Annual Reports in Medicinal Chemistry: Elsevier Science Inc [distributor]

Annual Reports in Medicinal Chemistry.: Elsevier Science Inc [distributor]

Annual Reports in Medicinal Chemistry

Annual Reports in Medicinal Chemistry

Annual Reports in Medicinal Chemistry

Annual Reports in Medicinal Chemistry

Annual Reports in Medicinal Chemistry

Facile synthesis of potent HIV-1 protease inhibitors containing a novel pseudo-symmetric dipeptide isostere

Synthesis of (±)-cycloprop-G, the cyclopropyl analogue of the broad spectrum antiviral agent cyclobut-G

Synthesis of (2S,5S,4R)-2,5-diamino-3,3-difluoro-1,6-diphenylhydroxyhexane : the core unit of a potent HIV proteinase inhibitor

Linear and Macrocyclic Hepatitis C Virus Protease Inhibitors: Inhibitor Design and Macrocyclization Strategies for HCV Protease and Related Targets

Profile of the Renin Inhibitor, Enalkiren (ABBOTT‐64662)

ChemInform Abstract: Discovery and Structure-Activity Study of a Novel Benzoxaborole Antiinflammatory Agent (AN2728) for the Potential Topical Treatment of Psoriasis and Atopic Dermatitis

Novel Lopinavir Analogues Incorporating Heterocyclic Replacements of Six-Member Cyclic Urea. Synthesis and Structure-Activity Relationships

ChemInform Abstract: Motilides and Motilactides: Design and Development of Motilin Receptor Agonists as a New Class of Gastrointestinal Prokinetic Drugs

Novel Lopinavir Analogues Incorporating Non-aromatic P-1 Side Chains - Synthesis and Structure-Activity Relationships

ChemInform Abstract: Synthesis and Structure-Activity Relationships of a Novel Series of HIV-1 Protease Inhibitors Encompassing ABT-378 (Lopinavir)

Chapter 7 Antihypertensive Agents

Synthesis and Activities of the Phosphonate Isostere of the Monophosphate of (±)Cyclobut-G

SECTION III: CANCER AND INFECTIOUS DISEASES

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