☰ Chemistry Tree

John A. Murphy, Ph.D

Affiliations:	1983-1995	Chemistry	University of Nottingham, Nottingham, England, United Kingdom
	1995-	Chemistry	University of Strathclyde, Glasgow, Scotland, United Kingdom

Area:

Organic chemistry

Website:

http://www.strath.ac.uk/chemistry/staff/academic/johnmurphy/

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Mean distance: 9.15

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Parents

grad student

1976-1980

Children

James John Crawford	research assistant	1999-1999	University of Strathclyde
Julia M. Dickinson	grad student		Nottingham
Mahesh Mohan	grad student		University of Strathclyde
Mick Sherburn	grad student	1991	Nottingham
Damien Bonne	grad student	2002-2003	University of Strathclyde
Franziska Schoenebeck	grad student	2004-2008	RWTH Aachen University
Joshua Philip Barham	grad student	2013-2017	University of Strathclyde
R. Vijaya Anand	post-doc	2004-2005	University of Strathclyde

Collaborators

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Publications

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Tyerman S, MacKay DG, Clark KF, et al. (2024) Monitoring Radical Intermediates in Photoactivated Palladium-Catalyzed Coupling of Aryl Halides to Arenes by an Aryl Radical Assay. Acs Catalysis. 15: 917-927
Clark KF, Murphy JA. (2024) Trio of radicals choreographed for versatile chemical reaction. Nature. 628: 42-43
Robb I, Murphy JA. (2024) Direct, Selective α-Aryloxyalkyl Radical Cyanation and Allylation of Aryl Alkyl Ethers. Organic Letters
Clark KF, Tyerman S, Evans L, et al. (2024) An assay for aryl radicals using BHAS coupling. Organic & Biomolecular Chemistry
Clark KF, Tyerman S, Evans L, et al. (2023) A Hierarchy of Ligands Controls Formation and Reaction of Aryl Radicals in Pd-Catalyzed Ground-State Base-Promoted Coupling Reactions. Journal of the American Chemical Society
Bell JD, Robb I, Murphy JA. (2022) Highly selective α-aryloxyalkyl C-H functionalisation of aryl alkyl ethers. Chemical Science. 13: 12921-12926
Pratley C, Fenner S, Murphy JA. (2022) Nitrogen-Centered Radicals in Functionalization of sp Systems: Generation, Reactivity, and Applications in Synthesis. Chemical Reviews
Kolodziejczak K, Stewart AJ, Tuttle T, et al. (2021) Radical and Ionic Mechanisms in Rearrangements of -Tolyl Aryl Ethers and Amines Initiated by the Grubbs-Stoltz Reagent, EtSiH/KOBu. Molecules (Basel, Switzerland). 26
Smith AJ, Dimitrova D, Arokianathar JN, et al. (2020) EtSiH + KO Bu provide multiple reactive intermediates that compete in the reactions and rearrangements of benzylnitriles and indolenines. Chemical Science. 11: 12364-12370
Smith AJ, Dimitrova D, Arokianathar JN, et al. (2020) New reductive rearrangement of -arylindoles triggered by the Grubbs-Stoltz reagent EtSiH/KO Bu. Chemical Science. 11: 3719-3726

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