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Alison E. Wendlandt
Researcher at University of Wisconsin-Madison
Publications - 23
Citations - 2327
Alison E. Wendlandt is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Catalysis & Quinone. The author has an hindex of 10, co-authored 19 publications receiving 2081 citations. Previous affiliations of Alison E. Wendlandt include University of Kentucky.
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Journal ArticleDOI
Copper-Catalyzed Aerobic Oxidative C ? H Functionalizations: Trends and Mechanistic Insights
TL;DR: This work has reported several recently reported Cu-catalyzed C-H oxidation reactions that feature substrates that are electron-deficient or appear unlikely to undergo single-electron transfer to copper(II), and evidence has been obtained for the involvement of organocopper(III) intermediates in the reaction mechanism.
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Quinone-Catalyzed Selective Oxidation of Organic Molecules
TL;DR: The collective observations show that the quinone structure has a significant influence on the reaction mechanism and has important implications for the development of new quin one reagents and quinOne-catalyzed transformations.
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Kupferkatalysierte aerobe oxidative C‐H‐Funktionalisierungen: Trends und Erkenntnisse zum Mechanismus
TL;DR: In this article, a set of new Cu-katalysierte C-H-Oxidationen with elektronenarmen substraten was given, of which one of them was a Kupfer(II)-Katalysator.
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Bioinspired aerobic oxidation of secondary amines and nitrogen heterocycles with a bifunctional quinone catalyst.
TL;DR: A novel bioinspired quinone catalyst system consisting of 1,10-phenanthroline-5,6-dione/ZnI2 that bypasses constraints via an abiological pathway involving a hemiaminal intermediate provides a valuable foundation for broader development of aerobic oxidation reactions employing quin one-based catalysts.
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Modular o-quinone catalyst system for dehydrogenation of tetrahydroquinolines under ambient conditions.
TL;DR: The design and development of new o-quinone-based catalysts for the oxidative dehydrogenation of tetrahydroquinolines to afford quinolines are reported, using a Co(salophen) cocatalyst for the reaction to proceed efficiently with ambient air at room temperature.