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New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction

Journal of the American Chemical Society, 2000-05, Vol.122 (17), p.4243-4244

2000

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A Concise Asymmetric Synthesis of the ADE Fragment of Nakadomarin A

Organic letters, 2004-11, Vol.6 (24), p.4539-4541

2004

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Annulation of Aromatic Imines via Directed C−H Bond Activation

Journal of organic chemistry, 2005-08, Vol.70 (17), p.6775-6781

2005

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A Noncompetitive Inhibitor for Mycobacterium tuberculosis’s Class IIa Fructose 1,6-Bisphosphate Aldolase

Biochemistry (Easton), 2014-01, Vol.53 (1), p.202-213

2014

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Pyrazolopyridine inhibitors of B-RafV600E. Part 3: An increase in aqueous solubility via the disruption of crystal packing

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (2), p.912-915

2012

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An Efficient Undergraduate Synthesis of the Exorbitantly Priced Lambert–Eaton Myasthenic Syndrome Drug Amifampridine

Journal of chemical education, 2023-02, Vol.100 (2), p.914-920

2023

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Pyrazolopyridine inhibitors of B-RafV600E. Part 2: Structure–activity relationships

Bioorganic & medicinal chemistry letters, 2011-09, Vol.21 (18), p.5533-5537

2011

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Pyrazolopyridine inhibitors of B-Raf(V600E). Part 3: an increase in aqueous solubility via the disruption of crystal packing

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (2), p.912-915

2012

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Synthesis of a Tricyclic Mescaline Analogue by Catalytic C−H Bond Activation

Organic letters, 2003-04, Vol.5 (8), p.1301-1303

2003

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The discovery of potent and selective pyridopyrimidin-7-one based inhibitors of B-RafV600E kinase

Bioorganic & medicinal chemistry letters, 2012-05, Vol.22 (10), p.3387-3391

2012

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A Concise Asymmetric Synthesis of the ADE Fragment of Nakadomarin A

Organic letters, 2005-03, Vol.7 (5), p.957-957

2005

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An Expedient Undergraduate Synthesis of Glycerol Phenylbutyrate, One of the Most Expensive Medications in the United States

Journal of chemical education, 2024-02, Vol.101 (2), p.578-586

2024

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Identification of potent and broad-Spectrum antibiotics from SAR studies of a synthetic vancomycin analogue

Bioorganic & medicinal chemistry letters, 2003-05, Vol.13 (10), p.1683-1686

2003

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A Noncompetitive Inhibitor for Mycobacterium tuberculosis ’s Class IIa Fructose 1,6-Bisphosphate Aldolase

Biochemistry (Easton), 2014-01, Vol.53 (1), p.202-213

2014

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Trityltitanium Complexes. X-ray Structural Characterization of [Ti(CO)4{η5-C(4-C6H4R)3}]- (R = H, OCH3)1

Organometallics, 1998-01, Vol.17 (1), p.13-15

1998

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Pyrazolopyridine inhibitors of B-Raf super(V600E. Part 2: Structure-activity relationships)

Bioorganic & medicinal chemistry letters, 2011-09, Vol.21 (18), p.5533-5537

2011

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Annulation of Aromatic Imines via Directed C-H BondActivation

Journal of organic chemistry, 2005-04, Vol.70

2005

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A Concise Asymmetric Synthesis of the ADE Fragment of Nakadomarin A

ChemInform, 2005-04, Vol.36 (15), p.no-no

2005

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Annulation of Aromatic Imines via Directed C-H Bond Activation

ChemInform, 2005-12, Vol.36 (52), p.no-no

2005

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ChemInform Abstract: New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels-Alder Reaction

ChemInform, 2000-08, Vol.31 (31), p.no-no

2000

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C-H Bond Activation by Iridium and Rhodium Complexes: Catalytic Hydrogen-Deuterium Exchange and C-C Bond-Forming Reactions

ChemInform, 2005-06, Vol.36 (24), p.no-no

2005

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Imidazo[4,5-b]pyridine inhibitors of B-Raf kinase

Bioorganic & medicinal chemistry letters, 2013-11, Vol.23 (21), p.5896-5899

2013

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New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction

A Concise Asymmetric Synthesis of the ADE Fragment of Nakadomarin A

Annulation of Aromatic Imines via Directed C−H Bond Activation

A Noncompetitive Inhibitor for Mycobacterium tuberculosis’s Class IIa Fructose 1,6-Bisphosphate Aldolase

Pyrazolopyridine inhibitors of B-RafV600E. Part 3: An increase in aqueous solubility via the disruption of crystal packing

An Efficient Undergraduate Synthesis of the Exorbitantly Priced Lambert–Eaton Myasthenic Syndrome Drug Amifampridine

Pyrazolopyridine inhibitors of B-RafV600E. Part 2: Structure–activity relationships

Pyrazolopyridine inhibitors of B-Raf(V600E). Part 3: an increase in aqueous solubility via the disruption of crystal packing

Synthesis of a Tricyclic Mescaline Analogue by Catalytic C−H Bond Activation

Pyrazolopyridine Inhibitors of B-Raf(V600E). Part 1: The Development of Selective, Orally Bioavailable, and Efficacious Inhibitors

The discovery of potent and selective pyridopyrimidin-7-one based inhibitors of B-RafV600E kinase

A Concise Asymmetric Synthesis of the ADE Fragment of Nakadomarin A

An Expedient Undergraduate Synthesis of Glycerol Phenylbutyrate, One of the Most Expensive Medications in the United States

Identification of potent and broad-Spectrum antibiotics from SAR studies of a synthetic vancomycin analogue

Pyrazolopyridine Inhibitors of B-RafV600E. Part 1: The Development of Selective, Orally Bioavailable, and Efficacious Inhibitors

A Noncompetitive Inhibitor for Mycobacterium tuberculosis ’s Class IIa Fructose 1,6-Bisphosphate Aldolase

Trityltitanium Complexes. X-ray Structural Characterization of [Ti(CO)4{η5-C(4-C6H4R)3}]- (R = H, OCH3)1

Pyrazolopyridine inhibitors of B-Raf super(V600E. Part 2: Structure-activity relationships)

Annulation of Aromatic Imines via Directed C-H BondActivation

Pyrazolopyridine Inhibitors of B-Raf V600E . Part 1: The Development of Selective, Orally Bioavailable, and Efficacious Inhibitors

A Concise Asymmetric Synthesis of the ADE Fragment of Nakadomarin A

Annulation of Aromatic Imines via Directed C-H Bond Activation

ChemInform Abstract: New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels-Alder Reaction

C-H Bond Activation by Iridium and Rhodium Complexes: Catalytic Hydrogen-Deuterium Exchange and C-C Bond-Forming Reactions

Imidazo[4,5-b]pyridine inhibitors of B-Raf kinase

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