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Liebeskind-Srogl C----C Cross-Coupling Reaction

Angewandte Chemie (International ed.), 2009-03, Vol.48 (13), p.2276-2286

2009

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Structural Basis for Inhibition of Eg5 by Dihydropyrimidines: Stereoselectivity of Antimitotic Inhibitors Enastron, Dimethylenastron and Fluorastrol

Journal of medicinal chemistry, 2010-08, Vol.53 (15), p.5676-5683

2010

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Copper-Catalyzed C----C Coupling of Thiol Esters and Boronic Acids under Aerobic Conditions

Angewandte Chemie (International ed.), 2008-05, Vol.47 (20), p.3674-3676

2008

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Ruthenium‐Catalyzed Reductive Arylation of N‐(2‐Pyridinyl)amides with Isopropanol and Arylboronate Esters

Angewandte Chemie International Edition, 2019-01, Vol.58 (2), p.482-487

International ed. in English, 2019

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The Role of the Alcohol and Carboxylic Acid in Directed Ruthenium-Catalyzed C(sp3)H α-Alkylation of Cyclic Amines

Chemistry : a European journal, 2012-08, Vol.18 (33), p.10393-10398

2012

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Microwave-assisted one-pot diboration/Suzuki cross-couplings. A rapid route to tetrasubstituted alkenes

Tetrahedron letters, 2008-08, Vol.49 (33), p.4831-4835

2008

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Palladium(0)-Catalyzed, Copper(I)-Mediated Coupling of Boronic Acids with Cyclic Thioamides. Selective Carbon−Carbon Bond Formation for the Functionalization of Heterocycles

Journal of organic chemistry, 2007-06, Vol.72 (12), p.4440-4448

2007

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The evolution of amidine-based brain penetrant BACE1 inhibitors

Bioorganic & medicinal chemistry letters, 2014-05, Vol.24 (9), p.2033-2045

2014

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C-2 Arylation of Piperidines through Directed Transition-Metal-Catalyzed sp3 CH Activation

Chemistry : a European journal, 2010-11, Vol.16 (44), p.13063-13067

2010

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Desulfitative Carbon-Carbon Cross-Coupling of Thioamide Fragments with Boronic Acids

Advanced synthesis & catalysis, 2007-02, Vol.349 (3), p.448-452

2007

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Structure-Activity Relationships and Molecular Docking of Novel Dihydropyrimidine-Based Mitotic Eg5 Inhibitors

ChemMedChem, 2010-10, Vol.5 (10), p.1760-1769

2010

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Synthesis of 5-Aroyldihydropyrimidinones via Liebeskind-Srogl Thiol Ester-Boronic Acid Cross-Couplings

Synlett, 2007-01, Vol.2007 (1), p.0043-0046

2007

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4-Cyano-6,7-dimethoxycarbostyrils with Solvent- and pH-Independent High Fluorescence Quantum Yields and Emission Maxima

European Journal of Organic Chemistry, 2008-01, Vol.2008 (3), p.563-571

2008

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Die C-C-Kreuzkupplung nach Liebeskind und Srogl

Angewandte Chemie, 2009-03, Vol.121 (13), p.2312-2322

2009

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Kupferkatalysierte C-C-Kupplung von Thiolestern und Boronsäuren unter aeroben Bedingungen

Angewandte Chemie, 2008-05, Vol.120 (20), p.3732-3734

2008

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Ruthenium‐Catalyzed Reductive Arylation of N‐(2‐Pyridinyl)amides with Isopropanol and Arylboronate Esters

Angewandte Chemie, 2019-01, Vol.131 (2), p.492-497

2019

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A Bayesian Approach to Kinetic Modeling of Accelerated Stability Studies and Shelf Life Determination

AAPS PharmSciTech, 2023-11, Vol.24 (8), p.250-250, Article 250

2023

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C‐2 Arylation of Piperidines through Directed Transition‐Metal‐Catalyzed sp 3 CH Activation

Chemistry : a European journal, 2010-11, Vol.16 (44), p.13063-13067

2010

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Die C‐C‐Kreuzkupplung nach Liebeskind und Srogl

Angewandte Chemie, 2009-03, Vol.121 (13), p.2312-2322

2009

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Kupferkatalysierte C‐C‐Kupplung von Thiolestern und Boronsäuren unter aeroben Bedingungen

Angewandte Chemie, 2008-05, Vol.120 (20), p.3732-3734

2008

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1,4-Oxazine β‑Secretase 1 (BACE1) Inhibitors: From Hit Generation to Orally Bioavailable Brain Penetrant Leads

Journal of medicinal chemistry, 2015-10, Vol.58 (20), p.8216-8235

2015

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Optimization of 1,4-Oxazine β‑Secretase 1 (BACE1) Inhibitors Toward a Clinical Candidate

Journal of medicinal chemistry, 2018-06, Vol.61 (12), p.5292-5303

2018

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Evaluation of a Series of β‑Secretase 1 Inhibitors Containing Novel Heteroaryl-Fused-Piperazine Amidine Warheads

ACS medicinal chemistry letters, 2019-08, Vol.10 (8), p.1159-1165

2019

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Correction to Optimization of 1,4-Oxazine β‑Secretase 1 (BACE1) Inhibitors Toward a Clinical Candidate

Journal of medicinal chemistry, 2018-12, Vol.61 (24), p.11415-11415

2018

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The Role of the Alcohol and Carboxylic Acid in Directed Ruthenium-Catalyzed C(sp3)H [alpha]-Alkylation of Cyclic Amines

Chemistry : a European journal, 2012-08, Vol.18 (33), p.10393

2012

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Liebeskind-Srogl C----C Cross-Coupling Reaction

Structural Basis for Inhibition of Eg5 by Dihydropyrimidines: Stereoselectivity of Antimitotic Inhibitors Enastron, Dimethylenastron and Fluorastrol

Copper-Catalyzed C----C Coupling of Thiol Esters and Boronic Acids under Aerobic Conditions

Ruthenium‐Catalyzed Reductive Arylation of N‐(2‐Pyridinyl)amides with Isopropanol and Arylboronate Esters

The Role of the Alcohol and Carboxylic Acid in Directed Ruthenium-Catalyzed C(sp3)H α-Alkylation of Cyclic Amines

Microwave-assisted one-pot diboration/Suzuki cross-couplings. A rapid route to tetrasubstituted alkenes

Palladium(0)-Catalyzed, Copper(I)-Mediated Coupling of Boronic Acids with Cyclic Thioamides. Selective Carbon−Carbon Bond Formation for the Functionalization of Heterocycles

The evolution of amidine-based brain penetrant BACE1 inhibitors

C-2 Arylation of Piperidines through Directed Transition-Metal-Catalyzed sp3 CH Activation

Desulfitative Carbon-Carbon Cross-Coupling of Thioamide Fragments with Boronic Acids

Structure-Activity Relationships and Molecular Docking of Novel Dihydropyrimidine-Based Mitotic Eg5 Inhibitors

Synthesis of 5-Aroyldihydropyrimidinones via Liebeskind-Srogl Thiol Ester-Boronic Acid Cross-Couplings

4-Cyano-6,7-dimethoxycarbostyrils with Solvent- and pH-Independent High Fluorescence Quantum Yields and Emission Maxima

Die C-C-Kreuzkupplung nach Liebeskind und Srogl

Kupferkatalysierte C-C-Kupplung von Thiolestern und Boronsäuren unter aeroben Bedingungen

Ruthenium‐Catalyzed Reductive Arylation of N‐(2‐Pyridinyl)amides with Isopropanol and Arylboronate Esters

A Bayesian Approach to Kinetic Modeling of Accelerated Stability Studies and Shelf Life Determination

C‐2 Arylation of Piperidines through Directed Transition‐Metal‐Catalyzed sp 3 CH Activation

Die C‐C‐Kreuzkupplung nach Liebeskind und Srogl

Kupferkatalysierte C‐C‐Kupplung von Thiolestern und Boronsäuren unter aeroben Bedingungen

1,4-Oxazine β‑Secretase 1 (BACE1) Inhibitors: From Hit Generation to Orally Bioavailable Brain Penetrant Leads

Optimization of 1,4-Oxazine β‑Secretase 1 (BACE1) Inhibitors Toward a Clinical Candidate

Evaluation of a Series of β‑Secretase 1 Inhibitors Containing Novel Heteroaryl-Fused-Piperazine Amidine Warheads

Correction to Optimization of 1,4-Oxazine β‑Secretase 1 (BACE1) Inhibitors Toward a Clinical Candidate

The Role of the Alcohol and Carboxylic Acid in Directed Ruthenium-Catalyzed C(sp3)H [alpha]-Alkylation of Cyclic Amines

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