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Jason G. Taylor

Researcher at Universidade Federal de Ouro Preto

Publications -  65
Citations -  1191

Jason G. Taylor is an academic researcher from Universidade Federal de Ouro Preto. The author has contributed to research in topics: Catalysis & Benznidazole. The author has an hindex of 14, co-authored 62 publications receiving 1031 citations. Previous affiliations of Jason G. Taylor include Imperial College London & State University of Campinas.

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Evolution And Synthetic Applications Of The Heck-matsuda Reaction: The Return Of Arenediazonium Salts To Prominence

TL;DR: In this paper, the authors highlight the potential and the versatility of arenediazonium salts as viable alternatives to conventional aryl halides and oxygen-based electrophiles for Pd-catalyzed Heck reactions.
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Copper-Catalyzed Intermolecular Hydroamination of Alkenes

TL;DR: Regioselective additions of arylsulfonamides to vinylarenes, norbornene, and cyclohexadiene were achieved using a copper-diphosphine catayst under mild reaction conditions and appear to be ligand-accelerated.
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Hydroamination reactions by metal triflates: Brønsted acid vs. metal catalysis?

TL;DR: Development in this field of catalytic research is briefly charted, followed by a discussion of possible mechanisms, including arguments to support the operation of both metal and Brønsted acid catalysis in these systems.
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Antioxidant, antimicrobial and anti-quorum sensing activities of Rubus rosaefolius phenolic extract

TL;DR: In this article, a study was conducted to characterize the centesimal composition, mineral and phenolic content, to determine the antioxidant and antimicrobial effect as well as the inhibition of quorum sensing by the phenolic extract obtained from wild strawberry ( Rubus rosaefolius ).
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Coumarins from Free ortho-Hydroxy Cinnamates by Heck-Matsuda Arylations: A Scalable Total Synthesis of (R)-Tolterodine

TL;DR: Free ortho-hydroxy cinnamate ester derivatives are evaluated in the synthesis of structurally diverse 4-aryl-coumarins via a tandem Heck-Matsuda cyclization reaction, which usually provides the corresponding diazo dyes.