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Catalytic Oxidative 1,2-Shift in 1,1′-Disubstituted Olefins Using Arene(iodo)sulfonic Acid as the Precatalyst and Oxone as the Oxidant

Organic letters, 2013-04, Vol.15 (7), p.1650-1653

2013

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Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic β-Lactones and Topology-Morphing Transformations

Angewandte Chemie (International ed.), 2010-12, Vol.49 (49), p.9479-9483

2010

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Development of a Process Route to the FAK/ALK Dual Inhibitor TEV-37440

Organic process research & development, 2017-05, Vol.21 (5), p.740-747

2017

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Concise Synthesis of Spirocyclic, Bridged γ-Butyrolactones via Stereospecific, Dyotropic Rearrangements of β-Lactones Involving 1,2-Acyl and δ-Lactone Migrations

Journal of the American Chemical Society, 2008-08, Vol.130 (32), p.10478-10479

2008

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Dyotropic Rearrangements of Fused Tricyclic β‑Lactones: Application to the Synthesis of (−)-Curcumanolide A and (−)-Curcumalactone

Journal of the American Chemical Society, 2012-08, Vol.134 (32), p.13348-13356

2012

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Bicyclic- and Tricyclic-β-lactones via Organonucleophile-Promoted Bis-Cyclizations of Keto Acids: Enantioselective Synthesis of (+)-Dihydroplakevulin

Organic letters, 2006-09, Vol.8 (19), p.4363-4366

2006

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Seven Important Elements for an Effective Green Chemistry Program: An IQ Consortium Perspective

Organic process research & development, 2013-09, Vol.17 (9), p.1099-1109

2013

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Practical, Catalytic, Asymmetric Synthesis of β-Lactones via a Sequential Ketene Dimerization/Hydrogenation Process: Inhibitors of the Thioesterase Domain of Fatty Acid Synthase

Journal of organic chemistry, 2006-06, Vol.71 (12), p.4549-4558

2006

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Correction to “Dyotropic Rearrangements of Fused Tricyclic β‑Lactones: Application to the Synthesis of (−)-Curcumanolide A and (−)-Curcumalactone”

Journal of the American Chemical Society, 2013-08, Vol.135 (33), p.12478-12478

2013

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One-step reductive amidation of nitro arenes: application in the synthesis of Acetaminophen

Tetrahedron letters, 2006-03, Vol.47 (11), p.1861-1864

2006

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Environmentally Friendly Solvent-Free Processes: Novel Dual Catalyst System in Henry Reaction

Organic process research & development, 2003-05, Vol.7 (3), p.254-258

2003

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Recent Advances in Lewis Base-Catalyzed, Stereoselective Tandem Aldol b- and g-Lactonizations

Heterocycles, 2008, Vol.76 (2), p.949

2008

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An Alternate Route to 2-Amino-3-nitro-5-bromo-4-picoline: Regioselective Pyridine Synthesis via 2-Nitramino-picoline Intermediate

Organic process research & development, 2007-09, Vol.11 (5), p.885-888

2007

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Benzoin Condensation: Monitoring a Chemical Reaction by High-Pressure Liquid Chromatography

Journal of chemical education, 2004-07, Vol.81 (7), p.1020

2004

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ChemInform Abstract: Catalytic Oxidative 1,2-Shift in 1,1′-Disubstituted Olefins Using Arene(iodo)sulfonic Acid as the Precatalyst and Oxone as the Oxidant

ChemInform, 2013-07, Vol.44 (31), p.no-no

2013

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Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic β-Lactones and Topology-Morphing Transformations

Angewandte Chemie, 2010-12, Vol.122 (49), p.9669-9673

2010

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Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic [beta]-Lactones and Topology-Morphing Transformations

Angewandte Chemie, 2010-12, Vol.122 (49), p.9669

2010

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ChemInform Abstract: Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic β-Lactones and Topology-Morphing Transformations

ChemInform, 2011-04, Vol.42 (15), p.no-no

2011

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ChemInform Abstract: Recent Advances in Lewis Base-Catalyzed, Stereoselective, Tandem Aldol β- and γ-Lactonizations

ChemInform, 2009-04, Vol.40 (14), p.no-no

2009

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ChemInform Abstract: Concise Synthesis of Spirocyclic, Bridged γ-Butyrolactones via Stereospecific, Dyotropic Rearrangements of β-Lactones Involving 1,2-Acyl and δ-Lactone Migrations

ChemInform, 2008-12, Vol.39 (52), p.no-no

2008

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Bicyclic- and Tricyclic -β-lactones via Organonucleophile-Promoted Bis-Cyclizations of Keto Acids: Enantioselective Synthesis of (+)-Dihydroplakevulin

ChemInform, 2007-01, Vol.38 (3), p.no-no

2007

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Practical, Catalytic, Asymmetric Synthesis of β-Lactones via a Sequential Ketene Dimerization/Hydrogenation Process: Inhibitors of the Thioesterase Domain of Fatty Acid Synthase

ChemInform, 2006-10, Vol.37 (41), p.no-no

2006

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One-Step Reductive Amidation of Nitro Arenes: Application in the Synthesis of Acetaminophen

ChemInform, 2006-06, Vol.37 (26), p.no-no

2006

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Chronic opioid antagonist treatment dose-dependently regulates μ-opioid receptors and trafficking proteins in vivo

Pharmacology, biochemistry and behavior, 2003-07, Vol.75 (4), p.909-913

2003

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Chronic opioid antagonist treatment selectively regulates trafficking and signaling proteins in mouse spinal cord

Synapse (New York, N.Y.), 2003-10, Vol.50 (1), p.67-76

2003

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Catalytic Oxidative 1,2-Shift in 1,1′-Disubstituted Olefins Using Arene(iodo)sulfonic Acid as the Precatalyst and Oxone as the Oxidant

Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic β-Lactones and Topology-Morphing Transformations

Development of a Process Route to the FAK/ALK Dual Inhibitor TEV-37440

Concise Synthesis of Spirocyclic, Bridged γ-Butyrolactones via Stereospecific, Dyotropic Rearrangements of β-Lactones Involving 1,2-Acyl and δ-Lactone Migrations

Dyotropic Rearrangements of Fused Tricyclic β‑Lactones: Application to the Synthesis of (−)-Curcumanolide A and (−)-Curcumalactone

Bicyclic- and Tricyclic-β-lactones via Organonucleophile-Promoted Bis-Cyclizations of Keto Acids: Enantioselective Synthesis of (+)-Dihydroplakevulin

Seven Important Elements for an Effective Green Chemistry Program: An IQ Consortium Perspective

Practical, Catalytic, Asymmetric Synthesis of β-Lactones via a Sequential Ketene Dimerization/Hydrogenation Process: Inhibitors of the Thioesterase Domain of Fatty Acid Synthase

Correction to “Dyotropic Rearrangements of Fused Tricyclic β‑Lactones: Application to the Synthesis of (−)-Curcumanolide A and (−)-Curcumalactone”

One-step reductive amidation of nitro arenes: application in the synthesis of Acetaminophen

Environmentally Friendly Solvent-Free Processes: Novel Dual Catalyst System in Henry Reaction

Recent Advances in Lewis Base-Catalyzed, Stereoselective Tandem Aldol b- and g-Lactonizations

An Alternate Route to 2-Amino-3-nitro-5-bromo-4-picoline: Regioselective Pyridine Synthesis via 2-Nitramino-picoline Intermediate

Benzoin Condensation: Monitoring a Chemical Reaction by High-Pressure Liquid Chromatography

ChemInform Abstract: Catalytic Oxidative 1,2-Shift in 1,1′-Disubstituted Olefins Using Arene(iodo)sulfonic Acid as the Precatalyst and Oxone as the Oxidant

Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic β-Lactones and Topology-Morphing Transformations

Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic [beta]-Lactones and Topology-Morphing Transformations

ChemInform Abstract: Enantioselective, Organocatalyzed, Intramolecular Aldol Lactonizations with Keto Acids Leading to Bi- and Tricyclic β-Lactones and Topology-Morphing Transformations

ChemInform Abstract: Recent Advances in Lewis Base-Catalyzed, Stereoselective, Tandem Aldol β- and γ-Lactonizations

ChemInform Abstract: Concise Synthesis of Spirocyclic, Bridged γ-Butyrolactones via Stereospecific, Dyotropic Rearrangements of β-Lactones Involving 1,2-Acyl and δ-Lactone Migrations

Bicyclic- and Tricyclic -β-lactones via Organonucleophile-Promoted Bis-Cyclizations of Keto Acids: Enantioselective Synthesis of (+)-Dihydroplakevulin

Practical, Catalytic, Asymmetric Synthesis of β-Lactones via a Sequential Ketene Dimerization/Hydrogenation Process: Inhibitors of the Thioesterase Domain of Fatty Acid Synthase

One-Step Reductive Amidation of Nitro Arenes: Application in the Synthesis of Acetaminophen

Chronic opioid antagonist treatment dose-dependently regulates μ-opioid receptors and trafficking proteins in vivo

Chronic opioid antagonist treatment selectively regulates trafficking and signaling proteins in mouse spinal cord

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