L
Luke R. Odell
Researcher at Uppsala University
Publications - 126
Citations - 2521
Luke R. Odell is an academic researcher from Uppsala University. The author has contributed to research in topics: Aryl & Catalysis. The author has an hindex of 27, co-authored 116 publications receiving 2150 citations. Previous affiliations of Luke R. Odell include University of Newcastle & Children's Medical Research Institute.
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Journal ArticleDOI
Molybdenum Hexacarbonyl Mediated CO Gas-Free Carbonylative Reactions
TL;DR: In this paper, the authors summarize their own experiences in developing microwave-heated palladium-catalyzed Mo(CO)6-mediated gas-free carbonylative reactions.
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Inhibition of dynamin mediated endocytosis by the dynoles--synthesis and functional activity of a family of indoles.
Timothy A. Hill,Christopher P. Gordon,Andrew B. McGeachie,Barbara Venn-Brown,Luke R. Odell,Ngoc Chau,Annie Quan,Anna Mariana,Jennette A. Sakoff,Megan Chircop,Phillip J. Robinson,Adam McCluskey +11 more
TL;DR: The dynoles represent a new series of tools to better probe endocytosis and dynamin-mediated trafficking events in a variety of cells and are the most active dynamin I inhibitors reported for in vitro or RME evaluations.
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Comprehensive mapping of neurotransmitter networks by MALDI-MS imaging.
Mohammadreza Shariatgorji,Mohammadreza Shariatgorji,Anna Nilsson,Anna Nilsson,Elva Fridjonsdottir,Theodosia Vallianatou,Patrik Källback,Luay Katan,Jonas Sävmarker,Ioannis Mantas,Xiaoqun Zhang,Erwan Bezard,Erwan Bezard,Per Svenningsson,Luke R. Odell,Per E. Andrén,Per E. Andrén +16 more
TL;DR: F fluoromethylpyridinium-based reactive matrices facilitate the covalent charge-tagging of molecules containing phenolic hydroxyl and/or primary or secondary amine groups, including dopaminergic and serotonergic neurotransmitters and their associated metabolites.
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Aminocarbonylations employing Mo(CO)6 and a bridged two-vial system: allowing the use of nitro group substituted aryl iodides and aryl bromides.
TL;DR: A bridged two-vial system aminocarbonylation protocol where Mo(CO)(6) functions as an external in situ solid source of CO has been developed and for the first time both nitro group containing aryl/heteroaryl iodides and bromides gave good to excellent yields.
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Functionalized 3-amino-imidazo[1,2-a]pyridines : A novel class of drug-like Mycobacterium tuberculosis glutamine synthetase inhibitors
Luke R. Odell,Mikael Nilsson,Johan Gising,Olof Lagerlund,Daniel Muthas,Anneli Nordqvist,Anders Karlén,Mats Larhed +7 more
TL;DR: 3-Amino-imidazo[1,2-a]pyridines have been identified as a novel class of Mycobacterium tuberculosis glutamine synthetase inhibitors and a series of compounds exploring structural diversity in the pyridine and phenyl rings have been synthesized and biologically evaluated.