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Thrombospondin-1 Mimetic Peptide Inhibitors of Angiogenesis and Tumor Growth: Design, Synthesis, and Optimization of Pharmacokinetics and Biological Activities

Journal of medicinal chemistry, 2005-04, Vol.48 (8), p.2838-2846

2005

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Structure−Activity Relationship Studies on N′-Aryl Carbohydrazide P2X7 Antagonists

Journal of medicinal chemistry, 2008-05, Vol.51 (10), p.3030-3034

2008

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Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X7 antagonists

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (14), p.4044-4048

2007

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Scaffold oriented synthesis. Part 4: Design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing heterocycle forming and multicomponent reactions

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (5), p.1480-1483

2011

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Discovery of a Series of Cyclohexylethylamine-Containing Protein Farnesyltransferase Inhibitors Exhibiting Potent Cellular Activity

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4844-4852

1999

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Scaffold oriented synthesis. Part 3: Design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing [2+3] cycloadditions

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (5), p.1476-1479

2011

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Microwave-Assisted Synthesis Utilizing Supported Reagents: A Rapid and Efficient Acylation Procedure

Organic letters, 2003-11, Vol.5 (24), p.4721-4724

2003

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Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (13), p.3574-3577

2006

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Novel Antibacterial Class: A Series of Tetracyclic Derivatives

Journal of medicinal chemistry, 2006-08, Vol.49 (16), p.4842-4856

2006

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Structure−Activity Relationship Studies on N ′-Aryl Carbohydrazide P2X 7 Antagonists

Journal of medicinal chemistry, 2008-05, Vol.51 (10), p.3030-3034

2008

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Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X sub(7) antagonists

Bioorganic & medicinal chemistry letters, 2007-07, Vol.17 (14), p.4044-4048

2007

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Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4 H-1,2,4-triazole P2X 7 antagonists

Bioorganic & medicinal chemistry letters, 2007, Vol.17 (14), p.4044-4048

2007

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Synthesis of (4R)-D,L-[4-2H]- and (4S)-D,L-[42H]homoserine lactones

Journal of organic chemistry, 1985-06, Vol.50 (13), p.2259-2263

1985

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Synthesis of (1S,2R)- and (1S,2S)-1-amino[2-2H]cyclopropane-1-carboxylic acids: The total 1H NMR assignment of cyclo[ACC-.alpha.-methyl-Phe]

Journal of organic chemistry, 1989-01, Vol.54 (2), p.270-276

1989

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Novel inhibitors of bacterial protein synthesis: structure–activity relationships for 1,8-naphthyridine derivatives incorporating position 3 and 4 variants

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3299-3302

2004

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Potent and Selective Non-Cysteine-Containing Inhibitors of Protein Farnesyltransferase

Journal of medicinal chemistry, 1998-10, Vol.41 (22), p.4288-4300

1998

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Potent and orally bioavailable noncysteine-containing inhibitors of protein farnesyltransferase

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (8), p.1069-1074

1999

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Preparation of 1-deuterioaldehydes via tub use of diisobutylaluminum deuteride (DIBAL-D)

Tetrahedron, 1984, Vol.40 (18), p.3387-3392

1984

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A practical large scale chemical synthesis of chiral glycines

Tetrahedron, 1988, Vol.44 (17), p.5597-5604

1988

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Microwave-Assisted Synthesis Utilizing Supported Reagents: A Rapid and Efficient Acylation Procedure

ChemInform, 2004-04, Vol.35 (14), p.no-no

2004

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A Facile Procedure for the Preparation of Alicyclic α-Amino Acids

Synthetic communications, 1985-03, Vol.15 (4), p.267-272

1985

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SYNTHESIS OF 4R- AND 4S- AND 3R- AND 3S-DEUTERATED HOMOSERINES. SYNTHESIS OF SPECIFICALLY-DEUTERATED 1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACIDS

KALVIN, DOUGLAS MARK

1985

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Novel and Potent 3‐(2,3‐Dichlorophenyl)‐4‐(benzyl)‐4H‐1,2,4‐triazole P2X 7 Antagonists

ChemInform, 2007-10, Vol.38 (44)

2007

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Assignment of the chemical shift values of N-trityl l-homoserine lactone

Tetrahedron letters, 1988, Vol.29 (33), p.4045-4048

1988

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Novel and Potent 3-(2,3-Dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X7 Antagonists

ChemInform, 2007-10, Vol.38 (44), p.no-no

2007

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Thrombospondin-1 Mimetic Peptide Inhibitors of Angiogenesis and Tumor Growth: Design, Synthesis, and Optimization of Pharmacokinetics and Biological Activities

Structure−Activity Relationship Studies on N′-Aryl Carbohydrazide P2X7 Antagonists

Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X7 antagonists

Scaffold oriented synthesis. Part 4: Design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing heterocycle forming and multicomponent reactions

Discovery of a Series of Cyclohexylethylamine-Containing Protein Farnesyltransferase Inhibitors Exhibiting Potent Cellular Activity

Scaffold oriented synthesis. Part 3: Design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing [2+3] cycloadditions

Microwave-Assisted Synthesis Utilizing Supported Reagents: A Rapid and Efficient Acylation Procedure

Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties

Novel Antibacterial Class: A Series of Tetracyclic Derivatives

Structure−Activity Relationship Studies on N ′-Aryl Carbohydrazide P2X 7 Antagonists

Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X sub(7) antagonists

Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4 H-1,2,4-triazole P2X 7 antagonists

Synthesis of (4R)-D,L-[4-2H]- and (4S)-D,L-[42H]homoserine lactones

Synthesis of (1S,2R)- and (1S,2S)-1-amino[2-2H]cyclopropane-1-carboxylic acids: The total 1H NMR assignment of cyclo[ACC-.alpha.-methyl-Phe]

Novel inhibitors of bacterial protein synthesis: structure–activity relationships for 1,8-naphthyridine derivatives incorporating position 3 and 4 variants

Potent and Selective Non-Cysteine-Containing Inhibitors of Protein Farnesyltransferase

Potent and orally bioavailable noncysteine-containing inhibitors of protein farnesyltransferase

Preparation of 1-deuterioaldehydes via tub use of diisobutylaluminum deuteride (DIBAL-D)

A practical large scale chemical synthesis of chiral glycines

Microwave-Assisted Synthesis Utilizing Supported Reagents: A Rapid and Efficient Acylation Procedure

A Facile Procedure for the Preparation of Alicyclic α-Amino Acids

SYNTHESIS OF 4R- AND 4S- AND 3R- AND 3S-DEUTERATED HOMOSERINES. SYNTHESIS OF SPECIFICALLY-DEUTERATED 1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACIDS

Novel and Potent 3‐(2,3‐Dichlorophenyl)‐4‐(benzyl)‐4H‐1,2,4‐triazole P2X 7 Antagonists

Assignment of the chemical shift values of N-trityl l-homoserine lactone

Novel and Potent 3-(2,3-Dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X7 Antagonists

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