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Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C–N Bond Activation

Journal of the American Chemical Society, 2017-04, Vol.139 (15), p.5313-5316

2017

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Vinylation of Benzylic Amines via C–N Bond Functionalization of Benzylic Pyridinium Salts

Synthesis (Stuttgart), 2018-08, Vol.50 (16), p.3231-3237

2018

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Harnessing Alkylpyridinium Salts as Electrophiles in Deaminative Alkyl–Alkyl Cross-Couplings

Journal of the American Chemical Society, 2019-02, Vol.141 (6), p.2257-2262

2019

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Nickel‐Catalyzed Synthesis of Dialkyl Ketones from the Coupling of N‐Alkyl Pyridinium Salts with Activated Carboxylic Acids

Angewandte Chemie International Edition, 2020-08, Vol.59 (32), p.13484-13489

International ed. in English, 2020

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Stereospecific Cross Couplings To Set Benzylic, All-Carbon Quaternary Stereocenters in High Enantiopurity

Journal of the American Chemical Society, 2016-09, Vol.138 (37), p.12057-12060

2016

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Nickel-Catalyzed Cross-Couplings of Benzylic Pivalates with Arylboroxines: Stereospecific Formation of Diarylalkanes and Triarylmethanes

Journal of the American Chemical Society, 2013-03, Vol.135 (9), p.3307-3310

2013

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Nickel-Catalyzed Borylation of Benzylic Ammonium Salts: Stereospecific Synthesis of Enantioenriched Benzylic Boronates

Organic letters, 2016-01, Vol.18 (1), p.136-139

2016

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Deaminative Reductive Cross-Electrophile Couplings of Alkylpyridinium Salts and Aryl Bromides

Organic letters, 2019-04, Vol.21 (8), p.2941-2946

2019

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Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives

Chemical communications (Cambridge, England), 2018-10, Vol.54 (87), p.12286-1231

2018

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Overcoming the Naphthyl Requirement in Stereospecific Cross-Couplings to Form Quaternary Stereocenters

Journal of the American Chemical Society, 2021-06, Vol.143 (23), p.8608-8613

2021

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Accessing Both Retention and Inversion Pathways in Stereospecific, Nickel-Catalyzed Miyaura Borylations of Allylic Pivalates

Journal of the American Chemical Society, 2016-09, Vol.138 (36), p.11989-11995

2016

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Enantioselective Copper(I)-Catalyzed Alkynylation of Oxocarbenium Ions to Set Diaryl Tetrasubstituted Stereocenters

Angewandte Chemie International Edition, 2015-11, Vol.54 (47), p.14154-14158

International ed. in English, 2015

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Nickel-Catalyzed, Stereospecific C–C and C–B Cross-Couplings via C–N and C–O Bond Activation

ACS catalysis, 2021-02, Vol.11 (3), p.1604-1612

2021

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The Once and Future Catalysts: How the Challenges of First-Row Transition-Metal Catalysis Grew to Become Strengths

Accounts of chemical research, 2024-09, Vol.57 (17), p.2451-2452

2024

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Assessing curricula contribution to sustainability more holistically: Experiences from the integration of curricula assessment and students' perceptions at the Georgia Institute of Technology

Journal of cleaner production, 2013-12, Vol.61, p.106-116

2013

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Nickel-Catalyzed Deaminative Cyanation: Nitriles and One-Carbon Homologation from Alkyl Amines

Organic letters, 2021-08, Vol.23 (16), p.6242-6245

2021

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Nickel-Catalyzed Cross Couplings of Benzylic Ammonium Salts and Boronic Acids: Stereospecific Formation of Diarylethanes via C–N Bond Activation

Journal of the American Chemical Society, 2013-01, Vol.135 (1), p.280-285

2013

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Asymmetric Intramolecular Arylcyanation of Unactivated Olefins via C−CN Bond Activation

Journal of the American Chemical Society, 2008-09, Vol.130 (38), p.12594-12595

2008

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Nickel(0)-Catalyzed Heck Cross-Coupling via Activation of Aryl C–OPiv Bonds

Organic letters, 2012-03, Vol.14 (5), p.1202-1205

2012

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Transforming Benzylic Amines into Diarylmethanes: Cross-Couplings of Benzylic Pyridinium Salts via C–N Bond Activation

Organic letters, 2018-05, Vol.20 (10), p.3030-3033

2018

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Copper-Catalyzed Enantioselective Additions to Oxocarbenium Ions: Alkynylation of Isochroman Acetals

Journal of the American Chemical Society, 2011-11, Vol.133 (43), p.17142-17145

2011

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Deaminative Reductive Methylation of Alkylpyridinium Salts

Organic letters, 2021-09, Vol.23 (18), p.7059-7063

2021

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Stitching two chiral centers with one catalyst

Science (American Association for the Advancement of Science), 2020-01, Vol.367 (6477), p.509-510

2020

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Diversifying Amino Acids and Peptides via Deaminative Reductive Cross-Couplings Leveraging High-Throughput Experimentation

Journal of the American Chemical Society, 2023-03, Vol.145 (10), p.5684-5695

2023

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Primary vs. secondary alkylpyridinium salts: a comparison under electrochemical and chemical reduction conditions

Faraday discussions, 2023-10, Vol.247, p.324-332

2023

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Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C–N Bond Activation

Vinylation of Benzylic Amines via C–N Bond Functionalization of Benzylic Pyridinium Salts

Harnessing Alkylpyridinium Salts as Electrophiles in Deaminative Alkyl–Alkyl Cross-Couplings

Nickel‐Catalyzed Synthesis of Dialkyl Ketones from the Coupling of N‐Alkyl Pyridinium Salts with Activated Carboxylic Acids

Stereospecific Cross Couplings To Set Benzylic, All-Carbon Quaternary Stereocenters in High Enantiopurity

Nickel-Catalyzed Cross-Couplings of Benzylic Pivalates with Arylboroxines: Stereospecific Formation of Diarylalkanes and Triarylmethanes

Nickel-Catalyzed Borylation of Benzylic Ammonium Salts: Stereospecific Synthesis of Enantioenriched Benzylic Boronates

Deaminative Reductive Cross-Electrophile Couplings of Alkylpyridinium Salts and Aryl Bromides

Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives

Overcoming the Naphthyl Requirement in Stereospecific Cross-Couplings to Form Quaternary Stereocenters

Accessing Both Retention and Inversion Pathways in Stereospecific, Nickel-Catalyzed Miyaura Borylations of Allylic Pivalates

Enantioselective Copper(I)-Catalyzed Alkynylation of Oxocarbenium Ions to Set Diaryl Tetrasubstituted Stereocenters

Nickel-Catalyzed, Stereospecific C–C and C–B Cross-Couplings via C–N and C–O Bond Activation

The Once and Future Catalysts: How the Challenges of First-Row Transition-Metal Catalysis Grew to Become Strengths

Assessing curricula contribution to sustainability more holistically: Experiences from the integration of curricula assessment and students' perceptions at the Georgia Institute of Technology

Nickel-Catalyzed Deaminative Cyanation: Nitriles and One-Carbon Homologation from Alkyl Amines

Nickel-Catalyzed Cross Couplings of Benzylic Ammonium Salts and Boronic Acids: Stereospecific Formation of Diarylethanes via C–N Bond Activation

Asymmetric Intramolecular Arylcyanation of Unactivated Olefins via C−CN Bond Activation

Nickel(0)-Catalyzed Heck Cross-Coupling via Activation of Aryl C–OPiv Bonds

Transforming Benzylic Amines into Diarylmethanes: Cross-Couplings of Benzylic Pyridinium Salts via C–N Bond Activation

Copper-Catalyzed Enantioselective Additions to Oxocarbenium Ions: Alkynylation of Isochroman Acetals

Deaminative Reductive Methylation of Alkylpyridinium Salts

Stitching two chiral centers with one catalyst

Diversifying Amino Acids and Peptides via Deaminative Reductive Cross-Couplings Leveraging High-Throughput Experimentation

Primary vs. secondary alkylpyridinium salts: a comparison under electrochemical and chemical reduction conditions

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