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Predicting reaction performance in C-N cross-coupling using machine learning

Science (American Association for the Advancement of Science), 2018-04, Vol.360 (6385), p.186-190

2018

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The importance of synthetic chemistry in the pharmaceutical industry

Science (American Association for the Advancement of Science), 2019-01, Vol.363 (6424)

2019

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Aryl amination using ligand-free Ni(II) salts and photoredox catalysis

Science (American Association for the Advancement of Science), 2016-07, Vol.353 (6296), p.279-283

2016

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Response to Comment on "Predicting reaction performance in C-N cross-coupling using machine learning"

Science (American Association for the Advancement of Science), 2018-11, Vol.362 (6416)

2018

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Nanomole-scale high-throughput chemistry for the synthesis of complex molecules

Science (American Association for the Advancement of Science), 2015-01, Vol.347 (6217), p.49-53

2015

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Palladium-Catalyzed C(sp3)–H Arylation of Diarylmethanes at Room Temperature: Synthesis of Triarylmethanes via Deprotonative-Cross-Coupling Processes

Journal of the American Chemical Society, 2012-08, Vol.134 (33), p.13765-13772

2012

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Palladium-Catalyzed, Direct Boronic Acid Synthesis from Aryl Chlorides: A Simplified Route to Diverse Boronate Ester Derivatives

Journal of the American Chemical Society, 2010-12, Vol.132 (50), p.17701-17703

2010

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Chemistry informer libraries: a chemoinformatics enabled approach to evaluate and advance synthetic methods

Chemical science (Cambridge), 2016-01, Vol.7 (4), p.2604-2613

2016

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Ultrasensitive microfluidic solid-phase ELISA using an actuatable microwell-patterned PDMS chip

Lab on a chip, 2013-11, Vol.13 (21), p.4190-4197

2013

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NiXantphos: A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides

Journal of the American Chemical Society, 2014-04, Vol.136 (17), p.6276-6287

2014

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Lysine specific demethylase 1 is a molecular driver and therapeutic target in sarcoma

Frontiers in oncology, 2023-01, Vol.12, p.1076581-1076581

2023

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Palladium-Catalyzed Enantioselective Arylation of Aryl Sulfenate Anions: A Combined Experimental and Computational Study

Journal of the American Chemical Society, 2017-06, Vol.139 (24), p.8337-8345

2017

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Scope of the Palladium-Catalyzed Aryl Borylation Utilizing Bis-Boronic Acid

Journal of the American Chemical Society, 2012-07, Vol.134 (28), p.11667-11673

2012

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P2Et Phosphazene: A Mild, Functional Group Tolerant Base for Soluble, Room Temperature Pd-Catalyzed C–N, C–O, and C–C Cross-Coupling Reactions

Organic letters, 2015-07, Vol.17 (13), p.3370-3373

2015

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Synthesis of Complex Druglike Molecules by the Use of Highly Functionalized Bench-Stable Organozinc Reagents

Angewandte Chemie (International ed.), 2016-10, Vol.55 (44), p.13714-13718

International ed. in English, 2016

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Copper-Facilitated Suzuki Reactions: Application to 2-Heterocyclic Boronates

Organic letters, 2009-01, Vol.11 (2), p.345-347

2009

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Asymmetric Cross-Coupling of Aryl Triflates to the Benzylic Position of Benzylamines

Angewandte Chemie (International ed.), 2012-11, Vol.51 (46), p.11510-11513

International ed. in English, 2012

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Practical guide on MALDI-TOF MS method development for high throughput profiling of pharmaceutically relevant, small molecule chemical reactions

Tetrahedron, 2020-09, Vol.76 (36), p.131434, Article 131434

2020

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Chemistry Informer Libraries: Conception, Early Experience, and Role in the Future of Cheminformatics

Accounts of chemical research, 2021-04, Vol.54 (7), p.1586-1596

2021

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Frequency and spatial distribution of cartilage thickness change in knee osteoarthritis and its relation to clinical and radiographic covariates – data from the osteoarthritis initiative

Osteoarthritis and cartilage, 2013-01, Vol.21 (1), p.102-109

2013

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The Open Reaction Database

Journal of the American Chemical Society, 2021-11, Vol.143 (45), p.18820-18826

2021

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Sensitivity to change of cartilage morphometry using coronal FLASH, sagittal DESS, and coronal MPR DESS protocols – comparative data from the osteoarthritis initiative (OAI)

Osteoarthritis and cartilage, 2010-04, Vol.18 (4), p.547-554

2010

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Accelerating reaction generality and mechanistic insight through additive mapping

Science (American Association for the Advancement of Science), 2022-04, Vol.376 (6592), p.532-539

2022

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Role of oxygen free radicals in cancer development

European Journal of Cancer, 1996, Vol.32 (1), p.30-38

1996

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Mapping the dark space of chemical reactions with extended nanomole synthesis and MALDI-TOF MS

Science (American Association for the Advancement of Science), 2018-08, Vol.361 (6402)

2018

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Predicting reaction performance in C-N cross-coupling using machine learning

The importance of synthetic chemistry in the pharmaceutical industry

Aryl amination using ligand-free Ni(II) salts and photoredox catalysis

Response to Comment on "Predicting reaction performance in C-N cross-coupling using machine learning"

Nanomole-scale high-throughput chemistry for the synthesis of complex molecules

Palladium-Catalyzed C(sp3)–H Arylation of Diarylmethanes at Room Temperature: Synthesis of Triarylmethanes via Deprotonative-Cross-Coupling Processes

Palladium-Catalyzed, Direct Boronic Acid Synthesis from Aryl Chlorides: A Simplified Route to Diverse Boronate Ester Derivatives

Chemistry informer libraries: a chemoinformatics enabled approach to evaluate and advance synthetic methods

Ultrasensitive microfluidic solid-phase ELISA using an actuatable microwell-patterned PDMS chip

NiXantphos: A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides

Lysine specific demethylase 1 is a molecular driver and therapeutic target in sarcoma

Palladium-Catalyzed Enantioselective Arylation of Aryl Sulfenate Anions: A Combined Experimental and Computational Study

Scope of the Palladium-Catalyzed Aryl Borylation Utilizing Bis-Boronic Acid

P2Et Phosphazene: A Mild, Functional Group Tolerant Base for Soluble, Room Temperature Pd-Catalyzed C–N, C–O, and C–C Cross-Coupling Reactions

Synthesis of Complex Druglike Molecules by the Use of Highly Functionalized Bench-Stable Organozinc Reagents

Copper-Facilitated Suzuki Reactions: Application to 2-Heterocyclic Boronates

Asymmetric Cross-Coupling of Aryl Triflates to the Benzylic Position of Benzylamines

Practical guide on MALDI-TOF MS method development for high throughput profiling of pharmaceutically relevant, small molecule chemical reactions

Chemistry Informer Libraries: Conception, Early Experience, and Role in the Future of Cheminformatics

Frequency and spatial distribution of cartilage thickness change in knee osteoarthritis and its relation to clinical and radiographic covariates – data from the osteoarthritis initiative

The Open Reaction Database

Sensitivity to change of cartilage morphometry using coronal FLASH, sagittal DESS, and coronal MPR DESS protocols – comparative data from the osteoarthritis initiative (OAI)

Accelerating reaction generality and mechanistic insight through additive mapping

Role of oxygen free radicals in cancer development

Mapping the dark space of chemical reactions with extended nanomole synthesis and MALDI-TOF MS

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