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Shauna M. Paradine

Researcher at Harvard University

Publications -  11
Citations -  694

Shauna M. Paradine is an academic researcher from Harvard University. The author has contributed to research in topics: Catalysis & Enantioselective synthesis. The author has an hindex of 5, co-authored 8 publications receiving 581 citations. Previous affiliations of Shauna M. Paradine include University of Illinois at Urbana–Champaign & Albion College.

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Journal ArticleDOI

Iron-catalyzed intramolecular allylic C-H amination.

TL;DR: Although this reaction is shown to proceed via a stepwise mechanism, the stereoretentive nature of C-H amination for 3° aliphatic C- H bonds suggests a very rapid radical rebound step.
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A manganese catalyst for highly reactive yet chemoselective intramolecular C( sp 3 )–H amination

TL;DR: A manganese catalyst is reported that aminates C–H bonds via a mechanism that lies between that of reactive noble metals (concerted) and chemoselective base metals (stepwise), demonstrating reactivity and selectivity unusual for previously known catalysts.
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Catalytic Enantioselective α‐Oxysulfonylation of Ketones Mediated by Iodoarenes

TL;DR: The alpha-oxysulfonylation of ketones catalysed by enantioenriched iodoarenes using mCPBA as stoichiometric oxidant is reported to give useful synthetic intermediates in good yield and modest enantioselectivity, believed to be the first report of an enantiOSElective organocatalytic reaction involving hypervalent iodine reagents.
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Enantioselective α-Oxytosylation of Ketones Catalysed by Iodoarenes

TL;DR: The α-oxytosylation of ketones catalysed by enantioen-riched iodoarenes using mCPBA as stoichiometric oxidant is reported to give useful synthetic intermediates in good yield and modest enantioselectivity, believed to be the first report of an enantiOSElective catalytic reaction involving hypervalent iodine reagents.
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Enantioselective, Catalytic Multicomponent Synthesis of Homoallylic Amines Enabled by Hydrogen-Bonding and Dispersive Interactions.

TL;DR: In this article, a one-step catalytic, enantioselective method for the preparation of homoallylic N-Boc amines directly from acetals is presented.