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Evolution of the Petasis−Ferrier Union/Rearrangement Tactic: Construction of Architecturally Complex Natural Products Possessing the Ubiquitous cis-2,6-Substituted Tetrahydropyran Structural Element

Accounts of chemical research, 2008-05, Vol.41 (5), p.675-687

2008

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A Preparatively Convenient Ligand-Free Catalytic PEG 2000 Suzuki−Miyaura Coupling

Journal of organic chemistry, 2009-02, Vol.74 (3), p.1381-1384

2009

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Development of a Practical Synthesis of Functionalized Azaxanthene-Derived Nonsteroidal Glucocorticoid Receptor Modulators

Organic process research & development, 2016-05, Vol.20 (5), p.921-933

2016

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Adventures in Atropisomerism: Total Synthesis of a Complex Active Pharmaceutical Ingredient with Two Chirality Axes

Organic letters, 2018-07, Vol.20 (13), p.3736-3740

2018

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(+)-Phorboxazole A Synthetic Studies. A Highly Convergent, Second Generation Total Synthesis of (+)-Phorboxazole A

Organic letters, 2005-09, Vol.7 (20), p.4399-4402

2005

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Systematic Optimization of a Robust Telescoped Process for a BTK Inhibitor with Atropisomer Control by High-Throughput Experimentation, Design of Experiments, and Linear Regression

Organic process research & development, 2019-06, Vol.23 (6), p.1143-1151

2019

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Development of a Kilogram-Scale Process for the Enantioselective Synthesis of 3‑Isopropenyl-cyclohexan-1-one via Rh/DTBM-SEGPHOS-Catalyzed Asymmetric Hayashi Addition Enabled by 1,3-Diol Additives

Organic process research & development, 2017-10, Vol.21 (10), p.1659-1667

2017

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Adventures in Atropisomerism: Development of a Robust, Diastereoselective, Lithium-Catalyzed Atropisomer-Forming Active Pharmaceutical Ingredient Step

Organic process research & development, 2018-10, Vol.22 (10), p.1426-1431

2018

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Scalability and Predictability of Polymorph Transformations Under High Shear

Organic process research & development, 2021-04, Vol.25 (4), p.1028-1035

2021

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A Second-Generation Total Synthesis of (+)-Phorboxazole A

Journal of organic chemistry, 2008-02, Vol.73 (4), p.1192-1200

2008

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Degradation Kinetics and Mechanism of an Oxadiazole Derivative, Design of a Stable Drug Product for BMS-708163, a γ-Secretase Inhibitor Drug Candidate

Journal of pharmaceutical sciences, 2012-09, Vol.101 (9), p.3124-3133

2012

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Synthesis and Biological Evaluation of Phorboxazole Congeners Leading to the Discovery and Preparative-Scale Synthesis of (+)-Chlorophorboxazole A Possessing Picomolar Human Solid Tumor Cell Growth Inhibitory Activity

Journal of organic chemistry, 2008-02, Vol.73 (4), p.1201-1208

2008

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Phorboxazole synthetic studies: design, synthesis and biological evaluation of phorboxazole A and hemi-phorboxazole A related analogues

Tetrahedron, 2011-07, Vol.67 (27), p.5069-5078

2011

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A Robust Three-Step Telescoped Synthesis of Electron- Deficient Amide Substituted Arylboronic Acids

Organic process research & development, 2011-03, Vol.15 (2), p.438-442

2011

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(+)-Phorboxazole A Synthetic Studies. Identification of a Series of Highly Cytotoxic C(45−46) Analogues

Organic letters, 2005-09, Vol.7 (20), p.4403-4406

2005

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Design and Synthesis of a Potent Phorboxazole C(11−15) Acetal Analogue

Organic letters, 2006-02, Vol.8 (4), p.797-799

2006

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Degradation kinetics and mechanism of an oxadiazole derivative, design of a stable drug product for BMS-708163, a [gamma]-secretase inhibitor drug candidate

Journal of pharmaceutical sciences, 2012-09, Vol.101 (9), p.3124

2012

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Phorboxazole synthetic studies: design, synthesis and biological evaluation of phorboxazole A and hemi-phorboxazole A related analogues: Strategies for the Synthesis of Tetrahydropyran-Containing Natural Products

Tetrahedron, 2011, Vol.67 (27-28)

2011

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Synthetic and biological studies of (+)-phorboxazole A: Second-generation total synthesis of (+)-phorboxazole A. Synthesis and biological evaluation of phorboxazole analogues. Progress toward the gram-scale synthesis of (+)-chlorophorboxazole A

Razler, Thomas M

2006

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ProQuest

ChemInform Abstract: Evolution of the Petasis-Ferrier Union/Rearrangement Tactic: Construction of Architecturally Complex Natural Products Possessing the Ubiquitous cis-2,6-Substituted Tetrahydropyran Structural Element

ChemInform, 2008-09, Vol.39 (37), p.no-no

2008

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(+)-Phorboxazole A Synthetic Studies. A Highly Convergent, Second Generation Total Synthesis of (+)-Phorboxazole A

ChemInform, 2006-02, Vol.37 (6), p.no-no

2006

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(+)-Phorboxazole A Synthetic Studies. Identification of a Series of Highly Cytotoxic C(45-46) Analogues

ChemInform, 2006-02, Vol.37 (6), p.no-no

2006

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Nickel-Catalyzed Synthesis of Quinazolinediones

Organic letters, 2017-03, Vol.19 (5), p.1052-1055

2017

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From Drying Kinetics, Solvate Structure, Particle Morphology, and Modeling to Optimal Drying Protocol

Organic process research & development, 2017-10, Vol.21 (10), p.1509-1520

2017

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Synthesis of pyrimido[4,5- b]indoles and benzo[4,5]furo[2,3- d]pyrimidines via palladium-catalyzed intramolecular arylation

Tetrahedron letters, 2002-11, Vol.43 (46), p.8235-8239

2002

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Evolution of the Petasis−Ferrier Union/Rearrangement Tactic: Construction of Architecturally Complex Natural Products Possessing the Ubiquitous cis-2,6-Substituted Tetrahydropyran Structural Element

A Preparatively Convenient Ligand-Free Catalytic PEG 2000 Suzuki−Miyaura Coupling

Development of a Practical Synthesis of Functionalized Azaxanthene-Derived Nonsteroidal Glucocorticoid Receptor Modulators

Adventures in Atropisomerism: Total Synthesis of a Complex Active Pharmaceutical Ingredient with Two Chirality Axes

(+)-Phorboxazole A Synthetic Studies. A Highly Convergent, Second Generation Total Synthesis of (+)-Phorboxazole A

Systematic Optimization of a Robust Telescoped Process for a BTK Inhibitor with Atropisomer Control by High-Throughput Experimentation, Design of Experiments, and Linear Regression

Development of a Kilogram-Scale Process for the Enantioselective Synthesis of 3‑Isopropenyl-cyclohexan-1-one via Rh/DTBM-SEGPHOS-Catalyzed Asymmetric Hayashi Addition Enabled by 1,3-Diol Additives

Adventures in Atropisomerism: Development of a Robust, Diastereoselective, Lithium-Catalyzed Atropisomer-Forming Active Pharmaceutical Ingredient Step

Scalability and Predictability of Polymorph Transformations Under High Shear

A Second-Generation Total Synthesis of (+)-Phorboxazole A

Degradation Kinetics and Mechanism of an Oxadiazole Derivative, Design of a Stable Drug Product for BMS-708163, a γ-Secretase Inhibitor Drug Candidate

Synthesis and Biological Evaluation of Phorboxazole Congeners Leading to the Discovery and Preparative-Scale Synthesis of (+)-Chlorophorboxazole A Possessing Picomolar Human Solid Tumor Cell Growth Inhibitory Activity

Phorboxazole synthetic studies: design, synthesis and biological evaluation of phorboxazole A and hemi-phorboxazole A related analogues

A Robust Three-Step Telescoped Synthesis of Electron- Deficient Amide Substituted Arylboronic Acids

(+)-Phorboxazole A Synthetic Studies. Identification of a Series of Highly Cytotoxic C(45−46) Analogues

Design and Synthesis of a Potent Phorboxazole C(11−15) Acetal Analogue

Degradation kinetics and mechanism of an oxadiazole derivative, design of a stable drug product for BMS-708163, a [gamma]-secretase inhibitor drug candidate

Phorboxazole synthetic studies: design, synthesis and biological evaluation of phorboxazole A and hemi-phorboxazole A related analogues: Strategies for the Synthesis of Tetrahydropyran-Containing Natural Products

Synthetic and biological studies of (+)-phorboxazole A: Second-generation total synthesis of (+)-phorboxazole A. Synthesis and biological evaluation of phorboxazole analogues. Progress toward the gram-scale synthesis of (+)-chlorophorboxazole A

ChemInform Abstract: Evolution of the Petasis-Ferrier Union/Rearrangement Tactic: Construction of Architecturally Complex Natural Products Possessing the Ubiquitous cis-2,6-Substituted Tetrahydropyran Structural Element

(+)-Phorboxazole A Synthetic Studies. A Highly Convergent, Second Generation Total Synthesis of (+)-Phorboxazole A

(+)-Phorboxazole A Synthetic Studies. Identification of a Series of Highly Cytotoxic C(45-46) Analogues

Nickel-Catalyzed Synthesis of Quinazolinediones

From Drying Kinetics, Solvate Structure, Particle Morphology, and Modeling to Optimal Drying Protocol

Synthesis of pyrimido[4,5- b]indoles and benzo[4,5]furo[2,3- d]pyrimidines via palladium-catalyzed intramolecular arylation

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