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Aromatic Cations from Oxidative Carbon–Hydrogen Bond Cleavage in Bimolecular Carbon–Carbon Bond Forming Reactions

Journal of organic chemistry, 2012-08, Vol.77 (15), p.6574-6582

2012

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Selective Electrochemical Oxidation of Functionalized Pyrrolidines

Organic letters, 2021-11, Vol.23 (22), p.8834-8837

2021

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Bimolecular coupling reactions through oxidatively generated aromatic cations: scope and stereocontrol

Tetrahedron, 2013-09, Vol.69 (36), p.7618-7626

2013

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Variable Active Site Loop Conformations Accommodate the Binding of Macrocyclic Largazole Analogues to HDAC8

Biochemistry (Easton), 2015-03, Vol.54 (12), p.2126-2135

2015

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Development of a selective HDAC inhibitor aimed at reactivating the HIV latent reservoir

Bioorganic & medicinal chemistry letters, 2020-09, Vol.30 (17), p.127367-127367, Article 127367

2020

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Modular synthesis and biological activity of pyridyl-based analogs of the potent Class I Histone Deacetylase Inhibitor Largazole

Bioorganic & medicinal chemistry, 2015-08, Vol.23 (15), p.5061-5074

2015

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Comparative pharmacokinetic properties and antitumor activity of the marine HDACi Largazole and Largazole peptide isostere

Cancer chemotherapy and pharmacology, 2015-04, Vol.75 (4), p.671-682

2015

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Total Synthesis of the Protein Phosphatase 2A Inhibitor Lactodehydrothyrsiferol

Angewandte Chemie, 2011-05, Vol.123 (22), p.5284-5287

2011

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Preparation of substituted 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepines from catalytic Cp∗Ir hydrogen transfer N-heterocyclization of anilino alcohols

Tetrahedron letters, 2006-09, Vol.47 (38), p.6899-6902

2006

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Discovery of ethyl ketone-based HDACs 1, 2, and 3 selective inhibitors for HIV latency reactivation

Bioorganic & medicinal chemistry letters, 2020-07, Vol.30 (13), p.127197-127197, Article 127197

2020

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Discovery of macrocyclic HDACs 1, 2, and 3 selective inhibitors for HIV latency reactivation

Bioorganic & medicinal chemistry letters, 2021-09, Vol.47, p.128168-128168, Article 128168

2021

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Discovery of Ethyl Ketone-Based Highly Selective HDACs 1, 2, 3 Inhibitors for HIV Latency Reactivation with Minimum Cellular Potency Serum Shift and Reduced hERG Activity

Journal of medicinal chemistry, 2021-04, Vol.64 (8), p.4709-4729

2021

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Total Synthesis of the Protein Phosphatase 2A Inhibitor Lactodehydrothyrsiferol

Angewandte Chemie, 2011-05, Vol.123 (22), p.5284-5287

2011

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Selective Class I HDAC Inhibitors Based on Aryl Ketone Zinc Binding Induce HIV‑1 Protein for Clearance

ACS medicinal chemistry letters, 2020-07, Vol.11 (7), p.1476-1483

2020

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Preparation of substituted 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1 H-benzo[ b][1,4]diazepines from catalytic Cp ∗Ir hydrogen transfer N-heterocyclization of anilino alcohols

Tetrahedron letters, 2006, Vol.47 (38), p.6899-6902

2006

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ChemInform Abstract: Bimolecular Coupling Reactions Through Oxidatively Generated Aromatic Cations: Scope and Stereocontrol

ChemInform, 2013-12, Vol.44 (52), p.no-no

2013

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Preparation of Substituted 1,2,3,4-Tetrahydroquinoxalines and 2,3,4,5-Tetrahydro-1H-benzo[b][1,4]diazepines from Catalytic CpIr Hydrogen Transfer N-Heterocyclization of Anilino Alcohols

ChemInform, 2007-01, Vol.38 (1), p.no-no

2007

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Gotthold Ephraim Lessings Verständnis des Judentums

Christentum und Judentum, 2012, Vol.24, p.157-176

2012

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Aromatic Cations from Oxidative Carbon–Hydrogen Bond Cleavage in Bimolecular Carbon–Carbon Bond Forming Reactions

Selective Electrochemical Oxidation of Functionalized Pyrrolidines

Bimolecular coupling reactions through oxidatively generated aromatic cations: scope and stereocontrol

Variable Active Site Loop Conformations Accommodate the Binding of Macrocyclic Largazole Analogues to HDAC8

Development of a selective HDAC inhibitor aimed at reactivating the HIV latent reservoir

Modular synthesis and biological activity of pyridyl-based analogs of the potent Class I Histone Deacetylase Inhibitor Largazole

Comparative pharmacokinetic properties and antitumor activity of the marine HDACi Largazole and Largazole peptide isostere

Total Synthesis of the Protein Phosphatase 2A Inhibitor Lactodehydrothyrsiferol

Preparation of substituted 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepines from catalytic Cp∗Ir hydrogen transfer N-heterocyclization of anilino alcohols

Discovery of ethyl ketone-based HDACs 1, 2, and 3 selective inhibitors for HIV latency reactivation

Discovery of macrocyclic HDACs 1, 2, and 3 selective inhibitors for HIV latency reactivation

Discovery of Ethyl Ketone-Based Highly Selective HDACs 1, 2, 3 Inhibitors for HIV Latency Reactivation with Minimum Cellular Potency Serum Shift and Reduced hERG Activity

Total Synthesis of the Protein Phosphatase 2A Inhibitor Lactodehydrothyrsiferol

Selective Class I HDAC Inhibitors Based on Aryl Ketone Zinc Binding Induce HIV‑1 Protein for Clearance

Preparation of substituted 1,2,3,4-tetrahydroquinoxalines and 2,3,4,5-tetrahydro-1 H-benzo[ b][1,4]diazepines from catalytic Cp ∗Ir hydrogen transfer N-heterocyclization of anilino alcohols

ChemInform Abstract: Bimolecular Coupling Reactions Through Oxidatively Generated Aromatic Cations: Scope and Stereocontrol

Preparation of Substituted 1,2,3,4-Tetrahydroquinoxalines and 2,3,4,5-Tetrahydro-1H-benzo[b][1,4]diazepines from Catalytic CpIr Hydrogen Transfer N-Heterocyclization of Anilino Alcohols

Gotthold Ephraim Lessings Verständnis des Judentums

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