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The role of flow in green chemistry and engineering

Green chemistry : an international journal and green chemistry resource : GC, 2013-01, Vol.15 (6), p.1456-1472

2013

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Enabling Tools and Techniques for Organic Synthesis: A Practical Guide to Experimentation, Automation, and Computation

Newman, Stephen G

1st edition, 2023

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High Throughput Strategies for the Discovery and Optimization of Catalytic Reactions

Angewandte Chemie (International ed.), 2019-05, Vol.58 (22), p.7180-7191

International ed. in English, 2019

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Methyl Esters as Cross-Coupling Electrophiles: Direct Synthesis of Amide Bonds

ACS catalysis, 2019-05, Vol.9 (5), p.4426-4433

2019

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Nickel‐Catalyzed Amide Bond Formation from Methyl Esters

Angewandte Chemie International Edition, 2018-09, Vol.57 (39), p.12925-12929

International ed. in English, 2018

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The Role of Reversible Oxidative Addition in Selective Palladium(0)-Catalyzed Intramolecular Cross-Couplings of Polyhalogenated Substrates: Synthesis of Brominated Indoles

Journal of the American Chemical Society, 2010-08, Vol.132 (33), p.11416-11417

2010

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A Cross-Coupling Approach to Amide Bond Formation from Esters

ACS catalysis, 2017-03, Vol.7 (3), p.2176-2180

2017

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Tools for chemical synthesis in microsystems

Lab on a chip, 2014-01, Vol.14 (17), p.326-3212

2014

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Switchable Selectivity in the Pd-Catalyzed Alkylative Cross-Coupling of Esters

Organic letters, 2018-07, Vol.20 (13), p.4094-4098

2018

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A Nickel‐Catalyzed Carbonyl‐Heck Reaction

Angewandte Chemie International Edition, 2017-11, Vol.56 (48), p.15441-15445

International ed. in English, 2017

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Nickel-catalyzed desulfonylative olefination of β-hydroxysulfones

Organic chemistry frontiers an international journal of organic chemistry, 2023-03, Vol.10 (6), p.1399-1404

2023

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Intramolecular cross-coupling of gem-dibromoolefins: a mild approach to 2-bromo benzofused heterocycles

Chemical communications (Cambridge, England), 2009-01 (35), p.5236-5238

2009

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Optimizing Chemical Reactions

Chemical reviews, 2024-04, Vol.124 (7), p.3645-3647

Newman, Stephen G.

2024

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Overcoming solid handling issues in continuous flow substitution reactions through ionic liquid formation

Green chemistry : an international journal and green chemistry resource : GC, 2018, Vol.20 (8), p.1748-1753

2018

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Palladium-Catalyzed Cross-Coupling of Superbase-Generated C(sp3) Nucleophiles

ACS catalysis, 2021-10, Vol.11 (19), p.12258-12263

2021

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Boron-Catalyzed Direct Aldol Reactions of Pyruvic Acids

Organic letters, 2009-12, Vol.11 (23), p.5486-5489

2009

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Alcohols as Substrates in Transition-Metal-Catalyzed Arylation, Alkylation, and Related Reactions

Chemical reviews, 2024-05, Vol.124 (9), p.6078-6144

2024

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Palladium-Catalyzed Carboiodination of Alkenes: Carbon−Carbon Bond Formation with Retention of Reactive Functionality

Journal of the American Chemical Society, 2011-02, Vol.133 (6), p.1778-1780

2011

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Enantioselective Rh-Catalyzed Domino Transformations of Alkynylcyclohexadienones with Organoboron Reagents

Organic letters, 2013-03, Vol.15 (5), p.1148-1151

2013

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Catalytic Aldehyde and Alcohol Arylation Reactions Facilitated by a 1,5-Diaza-3,7-diphosphacyclooctane Ligand

Journal of the American Chemical Society, 2021-09, Vol.143 (36), p.14646-14656

2021

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Palladium-Catalyzed Suzuki–Miyaura Coupling of Aryl Esters

Journal of the American Chemical Society, 2017-01, Vol.139 (3), p.1311-1318

2017

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Cross-coupling reactions with esters, aldehydes, and alcohols

Chemical communications (Cambridge, England), 2021-03, Vol.57 (21), p.2591-264

2021

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Nickel-Catalyzed Reductive Deoxygenation of Diverse C–O Bond-Bearing Functional Groups

ACS catalysis, 2021-11, Vol.11 (21), p.13337-13347

2021

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Nickel‐Catalyzed Domino Heck‐Type Reactions Using Methyl Esters as Cross‐Coupling Electrophiles

Angewandte Chemie International Edition, 2019-12, Vol.58 (50), p.18159-18164

International ed. in English, 2019

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An SN1‑Approach to Cross-Coupling: Deoxygenative Arylation Facilitated by the β‑Silicon Effect

Journal of the American Chemical Society, 2024-07, Vol.146 (29), p.19929-19938

2024

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The role of flow in green chemistry and engineering

Enabling Tools and Techniques for Organic Synthesis: A Practical Guide to Experimentation, Automation, and Computation

High Throughput Strategies for the Discovery and Optimization of Catalytic Reactions

Methyl Esters as Cross-Coupling Electrophiles: Direct Synthesis of Amide Bonds

Nickel‐Catalyzed Amide Bond Formation from Methyl Esters

The Role of Reversible Oxidative Addition in Selective Palladium(0)-Catalyzed Intramolecular Cross-Couplings of Polyhalogenated Substrates: Synthesis of Brominated Indoles

A Cross-Coupling Approach to Amide Bond Formation from Esters

Tools for chemical synthesis in microsystems

Switchable Selectivity in the Pd-Catalyzed Alkylative Cross-Coupling of Esters

A Nickel‐Catalyzed Carbonyl‐Heck Reaction

Nickel-catalyzed desulfonylative olefination of β-hydroxysulfones

Intramolecular cross-coupling of gem-dibromoolefins: a mild approach to 2-bromo benzofused heterocycles

Optimizing Chemical Reactions

Overcoming solid handling issues in continuous flow substitution reactions through ionic liquid formation

Palladium-Catalyzed Cross-Coupling of Superbase-Generated C(sp3) Nucleophiles

Boron-Catalyzed Direct Aldol Reactions of Pyruvic Acids

Alcohols as Substrates in Transition-Metal-Catalyzed Arylation, Alkylation, and Related Reactions

Palladium-Catalyzed Carboiodination of Alkenes: Carbon−Carbon Bond Formation with Retention of Reactive Functionality

Enantioselective Rh-Catalyzed Domino Transformations of Alkynylcyclohexadienones with Organoboron Reagents

Catalytic Aldehyde and Alcohol Arylation Reactions Facilitated by a 1,5-Diaza-3,7-diphosphacyclooctane Ligand

Palladium-Catalyzed Suzuki–Miyaura Coupling of Aryl Esters

Cross-coupling reactions with esters, aldehydes, and alcohols

Nickel-Catalyzed Reductive Deoxygenation of Diverse C–O Bond-Bearing Functional Groups

Nickel‐Catalyzed Domino Heck‐Type Reactions Using Methyl Esters as Cross‐Coupling Electrophiles

An SN1‑Approach to Cross-Coupling: Deoxygenative Arylation Facilitated by the β‑Silicon Effect

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