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Salt to Taste: The Critical Roles Played by Inorganic Salts in Organozinc Formation and in the Negishi Reaction

Angewandte Chemie International Edition, 2021-05, Vol.60 (22), p.12224-12241

International ed. in English, 2021

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Palladium Complexes of N-Heterocyclic Carbenes as Catalysts for Cross-Coupling Reactions-A Synthetic Chemist's Perspective

Angewandte Chemie (International ed.), 2007-01, Vol.46 (16), p.2768-2813

2007

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The Development of Bulky Palladium NHC Complexes for the Most-Challenging Cross-Coupling Reactions

Angewandte Chemie (International ed.), 2012-04, Vol.51 (14), p.3314-3332

International ed. in English, 2012

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Designing Pd–N-Heterocyclic Carbene Complexes for High Reactivity and Selectivity for Cross-Coupling Applications

Accounts of chemical research, 2017-09, Vol.50 (9), p.2244-2253

2017

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Carbon-Sulfur Bond Formation of Challenging Substrates at Low Temperature by Using Pd-PEPPSI-IPent

Chemistry : a European journal, 2011-10, Vol.17 (42), p.11719-11722

2011

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Sampling and Analysis in Flow: The Keys to Smarter, More Controllable, and Sustainable Fine‐Chemical Manufacturing

Angewandte Chemie International Edition, 2021-09, Vol.60 (38), p.20606-20626

International ed. in English, 2021

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Carbon–Heteroatom Coupling Using Pd-PEPPSI Complexes

Organic process research & development, 2014-01, Vol.18 (1), p.180-190

2014

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Pd-PEPPSI-IPent: Low-Temperature Negishi Cross-Coupling for the Preparation of Highly Functionalized, Tetra-ortho-Substituted Biaryls

Angewandte Chemie (International ed.), 2010-03, Vol.49 (11), p.2014-2017

2010

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What Industrial Chemists WantAre Academics Giving It to Them?

Organometallics, 2019-01, Vol.38 (1), p.66-75

2019

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Impact of N‐Aryl‐ and NHC Core‐Substituents on the Coupling of Alkylzinc Nucleophiles: Is Bigger always Better?

Chemistry : a European journal, 2022-06, Vol.28 (35), p.e202200665-n/a

2022

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Pd-PEPPSI-IPent: An Active, Sterically Demanding Cross-Coupling Catalyst and Its Application in the Synthesis of Tetra-Ortho-Substituted Biaryls

Angewandte Chemie (International ed.), 2009-01, Vol.48 (13), p.2383-2387

2009

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The Role of LiBr and ZnBr2 on the Cross‐Coupling of Aryl Bromides with Bu2Zn or BuZnBr

Chemistry : a European journal, 2019-12, Vol.25 (69), p.15751-15754

2019

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A Path to More Sustainable Catalysis: The Critical Role of LiBr in Avoiding Catalyst Death and its Impact on Cross‐Coupling

Chemistry : a European journal, 2020-04, Vol.26 (21), p.4861-4865

2020

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On The Remarkably Different Role of Salt in the Cross-Coupling of Arylzincs From That Seen With Alkylzincs

Angewandte Chemie (International ed.), 2014-04, Vol.53 (17), p.4386-4389

International ed. in English, 2014

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Potassium Isopropoxide: For Sulfination It is the Only Base You Need

Chemistry : a European journal, 2013-11, Vol.19 (48), p.16196-16199

2013

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Negishi cross-coupling of secondary alkylzinc halides with aryl/heteroaryl halides using Pd-PEPPSI-IPent

Chemical communications (Cambridge, England), 2011-01, Vol.47 (18), p.5181-5183

2011

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Sodium Butylated Hydroxytoluene: A Functional Group Tolerant, Eco‐Friendly Base for Solvent‐Free, Pd‐Catalysed Amination

Chemistry : a European journal, 2021-09, Vol.27 (49), p.12535-12539

2021

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Pd-PEPPSI Complexes and the Negishi Reaction

European Journal of Organic Chemistry, 2010-08, Vol.2010 (23), p.4343-4354

2010

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An Efficient Low-Temperature Stille-Migita Cross-Coupling Reaction for Heteroaromatic Compounds by Pd-PEPPSI-IPent

Chemistry : a European journal, 2010-04, Vol.16 (14), p.4279-4283

2010

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The Role of LiBr and ZnBr 2 on the Cross-Coupling of Aryl Bromides with Bu 2 Zn or BuZnBr

Chemistry : a European journal, 2019-12, Vol.25 (69), p.15751-15754

2019

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Murahashi Cross‐Coupling at −78 °C: A One‐Pot Procedure for Sequential C−C/C−C, C−C/C−N, and C−C/C−S Cross‐Coupling of Bromo‐Chloro‐Arenes

Chemistry : a European journal, 2019-07, Vol.25 (39), p.9180-9184

2019

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Pd-PEPPSI-IHept(Cl) : A General-Purpose, Highly Reactive Catalyst for the Selective Coupling of Secondary Alkyl Organozincs

Chemistry : a European journal, 2016-10, Vol.22 (41), p.14531-14534

2016

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Regioselective Cross-Coupling of Allylboronic Acid Pinacol Ester Derivatives with Aryl Halides via Pd-PEPPSI-IPent

Journal of the American Chemical Society, 2012-10, Vol.134 (42), p.17470-17473

2012

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Using Anilines as Masked Cross-Coupling Partners: Design of a Telescoped Three-Step Flow Diazotization, Iododediazotization, Cross-Coupling Process

Chemistry : a European journal, 2016-11, Vol.22 (48), p.17407-17415

2016

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Experimental and Computational Study on the Anti‐Markovnikov Hydrofunctionalization of Olefins Using Glycine‐Extended AQ‐Auxiliaries

Chemistry : a European journal, 2021-02, Vol.27 (11), p.3855-3860

2021

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Salt to Taste: The Critical Roles Played by Inorganic Salts in Organozinc Formation and in the Negishi Reaction

Palladium Complexes of N-Heterocyclic Carbenes as Catalysts for Cross-Coupling Reactions-A Synthetic Chemist's Perspective

The Development of Bulky Palladium NHC Complexes for the Most-Challenging Cross-Coupling Reactions

Designing Pd–N-Heterocyclic Carbene Complexes for High Reactivity and Selectivity for Cross-Coupling Applications

Carbon-Sulfur Bond Formation of Challenging Substrates at Low Temperature by Using Pd-PEPPSI-IPent

Sampling and Analysis in Flow: The Keys to Smarter, More Controllable, and Sustainable Fine‐Chemical Manufacturing

Carbon–Heteroatom Coupling Using Pd-PEPPSI Complexes

Pd-PEPPSI-IPent: Low-Temperature Negishi Cross-Coupling for the Preparation of Highly Functionalized, Tetra-ortho-Substituted Biaryls

What Industrial Chemists WantAre Academics Giving It to Them?

Impact of N‐Aryl‐ and NHC Core‐Substituents on the Coupling of Alkylzinc Nucleophiles: Is Bigger always Better?

Pd-PEPPSI-IPent: An Active, Sterically Demanding Cross-Coupling Catalyst and Its Application in the Synthesis of Tetra-Ortho-Substituted Biaryls

The Role of LiBr and ZnBr2 on the Cross‐Coupling of Aryl Bromides with Bu2Zn or BuZnBr

A Path to More Sustainable Catalysis: The Critical Role of LiBr in Avoiding Catalyst Death and its Impact on Cross‐Coupling

On The Remarkably Different Role of Salt in the Cross-Coupling of Arylzincs From That Seen With Alkylzincs

Potassium Isopropoxide: For Sulfination It is the Only Base You Need

Negishi cross-coupling of secondary alkylzinc halides with aryl/heteroaryl halides using Pd-PEPPSI-IPent

Sodium Butylated Hydroxytoluene: A Functional Group Tolerant, Eco‐Friendly Base for Solvent‐Free, Pd‐Catalysed Amination

Pd-PEPPSI Complexes and the Negishi Reaction

An Efficient Low-Temperature Stille-Migita Cross-Coupling Reaction for Heteroaromatic Compounds by Pd-PEPPSI-IPent

The Role of LiBr and ZnBr 2 on the Cross-Coupling of Aryl Bromides with Bu 2 Zn or BuZnBr

Murahashi Cross‐Coupling at −78 °C: A One‐Pot Procedure for Sequential C−C/C−C, C−C/C−N, and C−C/C−S Cross‐Coupling of Bromo‐Chloro‐Arenes

Pd-PEPPSI-IHept(Cl) : A General-Purpose, Highly Reactive Catalyst for the Selective Coupling of Secondary Alkyl Organozincs

Regioselective Cross-Coupling of Allylboronic Acid Pinacol Ester Derivatives with Aryl Halides via Pd-PEPPSI-IPent

Using Anilines as Masked Cross-Coupling Partners: Design of a Telescoped Three-Step Flow Diazotization, Iododediazotization, Cross-Coupling Process

Experimental and Computational Study on the Anti‐Markovnikov Hydrofunctionalization of Olefins Using Glycine‐Extended AQ‐Auxiliaries

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