M
Michael C. Willis
Researcher at University of Oxford
Publications - 227
Citations - 9016
Michael C. Willis is an academic researcher from University of Oxford. The author has contributed to research in topics: Catalysis & Hydroacylation. The author has an hindex of 50, co-authored 219 publications receiving 7587 citations. Previous affiliations of Michael C. Willis include University of Cambridge & Harvard University.
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Transition Metal Catalyzed Alkene and Alkyne Hydroacylation
TL;DR: Intermolecular Alkene Hydroacylation 3.2.1.
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Palladium-Catalyzed Aminosulfonylation of Aryl Halides
TL;DR: The palladium-catalyzed three-component coupling of aryl iodides, sulfur dioxide, and hydrazines to deliver aryll N-aminosulfonamides is described, and the reaction tolerates significant variation of both the aRYl iodide and Hydrazine coupling partners.
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The Development and Application of Sulfur Dioxide Surrogates in Synthetic Organic Chemistry
TL;DR: Sulfur dioxide surrogates have been used in a wide range of applications in chemistry, including traditional reactions in which the gaseous reagent has been replaced with a surrogate, and also new transformations for which no Gaseous reaction is known as discussed by the authors.
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DABCO-Bis(sulfur dioxide), DABSO, as a Convenient Source of Sulfur Dioxide for Organic Synthesis: Utility in Sulfonamide and Sulfamide Preparation
TL;DR: The charge-transfer complex generated from the combination of DABCO and sulfur dioxide, DABSO, is a bench-stable colorless solid suitable for use in organic synthesis as a replacement for gaseous sulfur dioxide.
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Palladium(II)‐Catalyzed Synthesis of Sulfinates from Boronic Acids and DABSO: A Redox‐Neutral, Phosphine‐Free Transformation
TL;DR: A redox‐neutral palladium(II)‐catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids into sulfinate intermediates, and onwards to sulfones and sulfonamides, has been realized.