Search Results - "Mackay, Emily G"

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  1. 1

    Electron-Catalyzed Fluoroalkylation of Vinyl Azides by Mackay, Emily G., Studer, Armido

    Published in Chemistry : a European journal (12-09-2016)
    “…The transition‐metal free fluoroalkylation of vinyl azides is herein reported. This operationally simple reaction employs the Togni reagent as a CF3 source,…”
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    Journal Article
  2. 2

    Demystifying the dendralenes by Mackay, Emily G., Sherburn, Michael S.

    Published in Pure and applied chemistry (15-05-2013)
    “…We present herein an overview of our ongoing studies with dendralenes. The first synthetic routes to this fundamental family of compounds have revealed…”
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    Journal Article
  3. 3

    Base-Promoted C–C Bond Activation Enables Radical Allylation with Homoallylic Alcohols by Lübbesmeyer, Maximilian, Mackay, Emily G, Raycroft, Mark A. R, Elfert, Jonas, Pratt, Derek A, Studer, Armido

    Published in Journal of the American Chemical Society (05-02-2020)
    “…The Cα–Cβ bond in homoallylic alcohols can be activated under basic conditions, qualifying these nonstrained acyclic systems as radical allylation reagents…”
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    Journal Article
  4. 4

    [5]Radialene by Mackay, Emily G, Newton, Christopher G, Toombs-Ruane, Henry, Lindeboom, Erik Jan, Fallon, Thomas, Willis, Anthony C, Paddon-Row, Michael N, Sherburn, Michael S

    Published in Journal of the American Chemical Society (25-11-2015)
    “…The [n]­radialenes are a unique family of fundamental [n]-membered carbocyclic structures with radiating alkenes, which have attracted significant synthetic…”
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    Journal Article
  5. 5

    Total Synthesis of Ramonanins A-D by Harvey, Ross S., Mackay, Emily G., Roger, Lukas, Paddon-Row, Michael N., Sherburn, Michael S., Lawrence, Andrew L.

    Published in Angewandte Chemie International Edition (02-02-2015)
    “…The first total synthesis of the ramonanin family of lignan natural products is described. The short synthesis involves a 2,5‐diaryl‐3,4‐dimethylene…”
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    Journal Article
  6. 6

    A Domino Diels–Alder Approach toward the Tetracyclic Nicandrenone Framework by Mackay, Emily G, Nörret, Marck, Wong, Leon S.-M, Louis, Ignace, Lawrence, Andrew L, Willis, Anthony C, Sherburn, Michael S

    Published in Organic letters (20-11-2015)
    “…The tetracarbocyclic framework of the nicandrenone natural products is formed in one step from a linear precursor via a domino intramolecular…”
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    Journal Article
  7. 7

    Preparation of an ion with the highest calculated proton affinity: ortho -diethynylbenzene dianion by Poad, Berwyck L J, Reed, Nicholas D, Hansen, Christopher S, Trevitt, Adam J, Blanksby, Stephen J, Mackay, Emily G, Sherburn, Michael S, Chan, Bun, Radom, Leo

    Published in Chemical science (Cambridge) (01-01-2016)
    “…Owing to the increased proton affinity that results from additional negative charges, multiply-charged anions have been proposed as one route to prepare and…”
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  8. 8

    Total Synthesis of RamonaninsA-D by Harvey, Ross S, Mackay, Emily G, Roger, Lukas, Paddon-Row, Michael N, Sherburn, Michael S, Lawrence, Andrew L

    Published in Angewandte Chemie International Edition (02-02-2015)
    “…The first total synthesis of the ramonanin family of lignan natural products is described. The short synthesis involves a 2,5-diaryl-3,4-dimethylene…”
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    Journal Article
  9. 9
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  11. 11

    Total Synthesis of RamonaninsA-D by Harvey, Ross S, Mackay, Emily G, Roger, Lukas, Paddon-Row, Michael N, Sherburn, Michael S, Lawrence, Andrew L

    Published in Angewandte Chemie (02-02-2015)
    “…The first total synthesis of the ramonanin family of lignan natural products is described. The short synthesis involves a 2,5-diaryl-3,4-dimethylene…”
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    Journal Article
  12. 12

    Total Synthesis of Ramonanins A-D by Harvey, Ross S., Mackay, Emily G., Roger, Lukas, Paddon-Row, Michael N., Sherburn, Michael S., Lawrence, Andrew L.

    Published in Angewandte Chemie (02-02-2015)
    “…The first total synthesis of the ramonanin family of lignan natural products is described. The short synthesis involves a 2,5‐diaryl‐3,4‐dimethylene…”
    Get full text
    Journal Article