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Introduction to small molecule drug discovery and preclinical development

Frontiers in drug discovery, 2023-11, Vol.3

2023

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Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation

Organic letters, 2016-04, Vol.18 (7), p.1562-1565

2016

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Investigating the Behavior of Published PAINS Alerts Using a Pharmaceutical Company Data Set

ACS medicinal chemistry letters, 2018-08, Vol.9 (8), p.792-796

2018

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Correction to “Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation”

Organic letters, 2016-05, Vol.18 (10), p.2519-2519

2016

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An Integrated Approach for Screening and Identification of Positive Allosteric Modulators of N-Methyl-D-Aspartate Receptors

Journal of biomolecular screening, 2016-06, Vol.21 (5), p.468-479

2016

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High affinity ligands for the α7 nicotinic receptor that show no cross-reactivity with the 5-HT3 receptor

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (21), p.4727-4730

2005

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High affinity ligands for the alpha7 nicotinic receptor that show no cross-reactivity with the 5-HT3 receptor

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (21), p.4727-4730

2005

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High affinity ligands for the α7 nicotinic receptor that show no cross-reactivity with the 5-HT 3 receptor

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (21), p.4727-4730

2005

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ChemInform Abstract: Diversely Substituted Quinolines via Rhodium‐Catalyzed Alkyne Hydroacylation

ChemInform, 2016-08, Vol.47 (35), p.no-no

2016

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Direct fluorination of the anthraquinone nucleus: scope and application to the synthesis of novel rhein analogues

Journal of fluorine chemistry, 1994-08, Vol.68 (2), p.201-203

1994

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Synthesis of 6/7-Halotetralones

Synthetic communications, 1991-04, Vol.21 (8-9), p.981-987

1991

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Anthraquinones related to rhein inhibit glucose uptake into chondrocytes. A mechanism for anti-osteoarthritis drugs?

Bioorganic & medicinal chemistry letters, 1997-04, Vol.7 (7), p.817-822

1997

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Synthesis of 6-tert-Butyl-2-Arylpyridines

Synthetic communications, 1992-01, Vol.22 (3), p.351-357

1992

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Synthesis of 4,5,8-trimethoxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid, an analogue of rhein with improved systemic exposure in the guinea pig

Journal of the Chemical Society, Perkin Transactions 1, 1995 (7), p.931

1995

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High Affinity Ligands for the α7 Nicotinic Receptor that Show no Cross-Reactivity with the 5-HT3 Receptor

ChemInform, 2006-01, Vol.37 (5), p.no-no

2006

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High Affinity Ligands for the α7 Nicotinic Receptor that Show no Cross‐Reactivity with the 5‐HT 3 Receptor

ChemInform, 2006-01, Vol.37 (5)

2006

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Introduction to small molecule drug discovery and preclinical development

Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation

Investigating the Behavior of Published PAINS Alerts Using a Pharmaceutical Company Data Set

Correction to “Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation”

An Integrated Approach for Screening and Identification of Positive Allosteric Modulators of N-Methyl-D-Aspartate Receptors

High affinity ligands for the α7 nicotinic receptor that show no cross-reactivity with the 5-HT3 receptor

High affinity ligands for the alpha7 nicotinic receptor that show no cross-reactivity with the 5-HT3 receptor

High affinity ligands for the α7 nicotinic receptor that show no cross-reactivity with the 5-HT 3 receptor

ChemInform Abstract: Diversely Substituted Quinolines via Rhodium‐Catalyzed Alkyne Hydroacylation

Direct fluorination of the anthraquinone nucleus: scope and application to the synthesis of novel rhein analogues

Synthesis of 6/7-Halotetralones

Anthraquinones related to rhein inhibit glucose uptake into chondrocytes. A mechanism for anti-osteoarthritis drugs?

Synthesis of 6-tert-Butyl-2-Arylpyridines

Synthesis of 4,5,8-trimethoxy-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid, an analogue of rhein with improved systemic exposure in the guinea pig

High Affinity Ligands for the α7 Nicotinic Receptor that Show no Cross-Reactivity with the 5-HT3 Receptor

High Affinity Ligands for the α7 Nicotinic Receptor that Show no Cross‐Reactivity with the 5‐HT 3 Receptor

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