Joshua A. Buss at Willard Henry Dow Laboratory Department of Chemistry University of Michigan 930 N. University Avenu - Research Interests, Publications & Academic Profile

Joshua A. Buss

University Name

United States

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Research Interests

Organic Chemistry

50%

Inorganic Chemistry

60%

Metal Chemistry

50%

Mechanistic Chemistry

40%

Catalysis

30%

Cycloaddition Reactions

30%

Supramolecular Chemistry

30%

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Articles10

Accessing Ta/Cu Architectures via Metal‐Metal Salt Metatheses: Heterobimetallic C−H Bond Activation Affords μ‐Hydrides

Article Link

Year:

2023

Synthesis, Structural Characterization, and CO2 Reactivity of a Constitutionally Analogous Series of Tricopper Mono-, Di-, and Trihydrides

Article Link

Year:

2023

Molybdenum-Mediated Coupling of Carbon Monoxide to a C3 Product on a Single Metal Site

Article Link

Year:

2022

Cu-Catalyzed Site-Selective Benzylic Chlorination Enabling Net C–H Coupling with Oxidatively Sensitive Nucleophiles

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Year:

2022

Carbon Dioxide Reduction with Dihydrogen and Silanes at Low-Valent Molybdenum Terphenyl Diphosphine Complexes: Reductant Identity Dictates Mechanism

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Year:

2021

Terminal, Open-Shell Mo Carbide and Carbyne Complexes: Spin Delocalization and Ligand Noninnocence

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Year:

2021

A hemilabile diphosphine pyridine pincer ligand: σ- and π-binding in molybdenum coordination complexes

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Year:

2020

Copper-Catalyzed C–H Fluorination/Functionalization Sequence Enabling Benzylic C–H Cross Coupling with Diverse Nucleophiles

Article Link

Year:

2020

Copper-Catalyzed Functionalization of Benzylic C–H Bonds with N-Fluorobenzenesulfonimide: Switch from C–N to C–F Bond Formation Promoted by a Redox Buffer and Brønsted Base

Article Link

Year:

2020

Copper-catalysed benzylic C–H coupling with alcohols via radical relay enabled by redox buffering

Article Link

Year:

2020

Collaborators1

Gwendolyn Bailey

Faculty, Assistant Professor

University of Minnesota

UNITED STATES

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Joshua A. Buss

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Research Interests

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Articles10

Accessing Ta/Cu Architectures via Metal‐Metal Salt Metatheses: Heterobimetallic C−H Bond Activation Affords μ‐Hydrides

Synthesis, Structural Characterization, and CO<sub>2</sub> Reactivity of a Constitutionally Analogous Series of Tricopper Mono-, Di-, and Trihydrides

Molybdenum-Mediated Coupling of Carbon Monoxide to a C<sub>3</sub> Product on a Single Metal Site

Cu-Catalyzed Site-Selective Benzylic Chlorination Enabling Net C–H Coupling with Oxidatively Sensitive Nucleophiles

Carbon Dioxide Reduction with Dihydrogen and Silanes at Low-Valent Molybdenum Terphenyl Diphosphine Complexes: Reductant Identity Dictates Mechanism

Terminal, Open-Shell Mo Carbide and Carbyne Complexes: Spin Delocalization and Ligand Noninnocence

A hemilabile diphosphine pyridine pincer ligand: σ- and π-binding in molybdenum coordination complexes

Copper-Catalyzed C–H Fluorination/Functionalization Sequence Enabling Benzylic C–H Cross Coupling with Diverse Nucleophiles

Copper-Catalyzed Functionalization of Benzylic C–H Bonds with <i>N</i>-Fluorobenzenesulfonimide: Switch from C–N to C–F Bond Formation Promoted by a Redox Buffer and Brønsted Base

Copper-catalysed benzylic C–H coupling with alcohols via radical relay enabled by redox buffering

Collaborators1

Gwendolyn Bailey

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