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Mechanistic Rationalization of Unusual Kinetics in Pd-Catalyzed C–H Olefination

Journal of the American Chemical Society, 2012-03, Vol.134 (10), p.4600-4606

2012

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Structure-Based Rationale for Selectivity in the Asymmetric Allylic Alkylation of Cycloalkenyl Esters Employing the Trost ‘Standard Ligand’ (TSL): Isolation, Analysis and Alkylation of the Monomeric form of the Cationic η3-Cyclohexenyl Complex [(η3-c-C6H9)Pd(TSL)]

Journal of the American Chemical Society, 2009-07, Vol.131 (29), p.9945-9957

2009

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Application of Multiple Kinetic Approaches to Understand Catalyst Stability in the Presence of Rapid Impurity-Mediated Deactivation

Topics in catalysis, 2017-06, Vol.60 (8), p.564-569

2017

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Structure-based rationale for selectivity in the asymmetric allylic alkylation of cycloalkenyl esters employing the Trost 'Standard Ligand' (TSL): isolation, analysis and alkylation of the monomeric form of the cationic eta(3)-cyclohexenyl complex [(eta(3)-c-C6H9)Pd(TSL)]

Journal of the American Chemical Society, 2009-07, Vol.131 (29), p.9945-9957

2009

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Mechanistic Studies on the Copper-Catalyzed N‑Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases

ACS catalysis, 2016-06, Vol.6 (6), p.3965-3974

2016

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A robust protocol for Pd(ii)-catalyzed C-3 arylation of (1H) indazoles and pyrazoles: total synthesis of nigellidine hydrobromide

Chemical science (Cambridge), 2013-01, Vol.4 (6), p.2374

2013

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Direct ortho-Arylation of Pyridinecarboxylic Acids: Overcoming the Deactivating Effect of sp2‑Nitrogen

Organic letters, 2016-12, Vol.18 (23), p.6094-6097

2016

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Electrospray Mass Spectrometric Studies of Two Palladium−Allyl Complexes of the Trost Standard Ligand

Organometallics, 2010-09, Vol.29 (17), p.3979-3986

2010

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Base-free, tunable, Au-catalyzed oxidative esterification of alcohols in continuous flow

Reaction chemistry & engineering, 2018-12, Vol.3 (6), p.942-948

2018

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Cleavage of tert -Butyl Benzoates with NaH in DMF: Comments on the Mechanism and a Simple and Safe Alternative Procedure

Synlett, 2009-01, Vol.2009 (2), p.205-208

2009

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Mechanistic and Performance Studies on the Ligand-Promoted Ullmann Amination Reaction

ACS catalysis, 2018-01, Vol.8 (1), p.101-109

2018

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New Insights into the Reaction Capabilities of Ionic Organic Bases in Cu‐Catalyzed Amination

European journal of organic chemistry, 2019-03, Vol.2019 (9), p.1944-1951

2019

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Hydroarylation of Alkenes by Protonation/Friedel–Crafts Trapping: HFIP-Mediated Access to Per-aryl Quaternary Stereocenters

Journal of organic chemistry, 2019-11, Vol.84 (22), p.14965-14973

2019

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Reversibility and reactivity in an acid catalyzed cyclocondensation to give furanochromanes - a reaction at the 'oxonium-Prins' vs. 'ortho-quinone methide cycloaddition' mechanistic nexusElectronic supplementary information (ESI) available: C. D.-T. Nielsen, W. J. Mooij, D. Sale, H. S. Rzepa, J. Burés and A. C. Spivey, FAIR data archives, Imperial College Research Computing Services data repository, 2018, DOI: 10.14469/hpc/3943 and sub-collections therein. See DOI: 10.1039/c8sc04302g

2019-01

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Reversibility and reactivity in an acid catalyzed cyclocondensation to give furanochromanes - a reaction at the 'oxonium-Prins' vs. ' ortho -quinone methide cycloaddition' mechanistic nexus

Chemical science (Cambridge), 2019-01, Vol.10 (2), p.406-412

2019

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Reversibility and reactivity in an acid catalyzed cyclocondensation to give furanochromanes – a reaction at the ‘oxonium-Prins’ vs. ‘ortho-quinone methide cycloaddition’ mechanistic nexus† †Electronic supplementary information (ESI) available: C. D.-T. Nielsen, W. J. Mooij, D. Sale, H. S. Rzepa, J. Burés and A. C. Spivey, FAIR data archives, Imperial College Research Computing Services data repository, 2018, DOI: 10.14469/hpc/3943 and sub-collections therein. See DOI: 10.1039/c8sc04302g

Chemical science (Cambridge), 2018-10, Vol.10 (2), p.406-412

2018

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Direct ortho-Arylation of Pyridinecarboxylic Acids: Overcoming the Deactivating Effect of sp 2 -Nitrogen

Organic letters, 2016-12, Vol.18 (23), p.6094-6097

2016

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Synthesis, Characterisation and Reactivity of Copper(I) Amide Complexes and Studies on Their Role in the Modified Ullmann Amination Reaction

Chemistry : a European journal, 2015-05, Vol.21 (19), p.7179-7192

2015

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A preliminary investigation into a rationally designed catalytic system for the epoxidation of alkenes based on a bipyridyl core

Journal of molecular catalysis. A, Chemical, 2008-12, Vol.296 (1), p.1-8

2008

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Structure-Based Rationale for Selectivity in the Asymmetric Allylic Alkylation of Cycloalkenyl Esters Employing the Trost ‘Standard Ligand’ (TSL): Isolation, Analysis and Alkylation of the Monomeric form of the Cationic η 3 -Cyclohexenyl Complex [(η 3 - c -C 6 H 9 )Pd(TSL)]

Journal of the American Chemical Society, 2009-07, Vol.131 (29), p.9945-9957

2009

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Interrogation of a dynamic multi-catalyst ensemble in asymmetric catalysis

Faraday discussions, 2010, Vol.145, p.27-47

2010

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Interrogation of a dynamic multi-catalyst ensemble in asymmetric catalysisElectronic supplementary information (ESI) available: Experimental details. CCDC reference number 733391. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b910022a

2010-01

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Base-free, tunable, Au-catalyzed oxidative esterification of alcohols in continuous flowElectronic supplementary information (ESI) available: Additional experimental procedure, characterization of reactor, catalysts, and data. See DOI: 10.1039/c8re00085a

2018-11

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Objectively measured free-living physical activity in pet dogs: Relationship to body condition score and owner-pet activity

Weber, David Isaiah Sale

2011

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ChemInform Abstract: A Robust Protocol for Pd(II)-Catalyzed C-3 Arylation of (1H) Indazoles and Pyrazoles: Total Synthesis of Nigellidine Hydrobromide

ChemInform, 2013-11, Vol.44 (45), p.no-no

2013

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Mechanistic Rationalization of Unusual Kinetics in Pd-Catalyzed C–H Olefination

Structure-Based Rationale for Selectivity in the Asymmetric Allylic Alkylation of Cycloalkenyl Esters Employing the Trost ‘Standard Ligand’ (TSL): Isolation, Analysis and Alkylation of the Monomeric form of the Cationic η3-Cyclohexenyl Complex [(η3-c-C6H9)Pd(TSL)]

Application of Multiple Kinetic Approaches to Understand Catalyst Stability in the Presence of Rapid Impurity-Mediated Deactivation

Structure-based rationale for selectivity in the asymmetric allylic alkylation of cycloalkenyl esters employing the Trost 'Standard Ligand' (TSL): isolation, analysis and alkylation of the monomeric form of the cationic eta(3)-cyclohexenyl complex [(eta(3)-c-C6H9)Pd(TSL)]

Mechanistic Studies on the Copper-Catalyzed N‑Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases

A robust protocol for Pd(ii)-catalyzed C-3 arylation of (1H) indazoles and pyrazoles: total synthesis of nigellidine hydrobromide

Direct ortho-Arylation of Pyridinecarboxylic Acids: Overcoming the Deactivating Effect of sp2‑Nitrogen

Electrospray Mass Spectrometric Studies of Two Palladium−Allyl Complexes of the Trost Standard Ligand

Base-free, tunable, Au-catalyzed oxidative esterification of alcohols in continuous flow

Cleavage of tert -Butyl Benzoates with NaH in DMF: Comments on the Mechanism and a Simple and Safe Alternative Procedure

Mechanistic and Performance Studies on the Ligand-Promoted Ullmann Amination Reaction

New Insights into the Reaction Capabilities of Ionic Organic Bases in Cu‐Catalyzed Amination

Hydroarylation of Alkenes by Protonation/Friedel–Crafts Trapping: HFIP-Mediated Access to Per-aryl Quaternary Stereocenters

Reversibility and reactivity in an acid catalyzed cyclocondensation to give furanochromanes - a reaction at the 'oxonium-Prins' vs. ' ortho -quinone methide cycloaddition' mechanistic nexus

Direct ortho-Arylation of Pyridinecarboxylic Acids: Overcoming the Deactivating Effect of sp 2 -Nitrogen

Synthesis, Characterisation and Reactivity of Copper(I) Amide Complexes and Studies on Their Role in the Modified Ullmann Amination Reaction

A preliminary investigation into a rationally designed catalytic system for the epoxidation of alkenes based on a bipyridyl core

Structure-Based Rationale for Selectivity in the Asymmetric Allylic Alkylation of Cycloalkenyl Esters Employing the Trost ‘Standard Ligand’ (TSL): Isolation, Analysis and Alkylation of the Monomeric form of the Cationic η 3 -Cyclohexenyl Complex [(η 3 - c -C 6 H 9 )Pd(TSL)]

Interrogation of a dynamic multi-catalyst ensemble in asymmetric catalysis

Interrogation of a dynamic multi-catalyst ensemble in asymmetric catalysisElectronic supplementary information (ESI) available: Experimental details. CCDC reference number 733391. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b910022a

Base-free, tunable, Au-catalyzed oxidative esterification of alcohols in continuous flowElectronic supplementary information (ESI) available: Additional experimental procedure, characterization of reactor, catalysts, and data. See DOI: 10.1039/c8re00085a

Objectively measured free-living physical activity in pet dogs: Relationship to body condition score and owner-pet activity

ChemInform Abstract: A Robust Protocol for Pd(II)-Catalyzed C-3 Arylation of (1H) Indazoles and Pyrazoles: Total Synthesis of Nigellidine Hydrobromide

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