2020

"Primary sulfonamide synthesis using the sulfinylamine reagent N-sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO", Thomas Q. Davies, Michael J. Tilby, David Skolc, Adrian Hall, and Michael C. Willis, Org. Lett202022, 9495–9499. (doi: 10.1021/acs.orglett.0c03505)

 

Highlighted on/in ChemistryViewsSynFacts, and the Organic Chemistry Portal.

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154 ga

 

"The 2-pyridyl problem: Challenging nucleophiles in cross-coupling arylations", Xinlan A. F. Cook, Antoine de Gombert, Janette McKnight, Loïc R. E. Pantaine and Michael C. Willis, Angew. Chem. Int. Ed. 202160, 11068–11091. (doi: 10.1002/anie.202010631

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153 ga

 

"Harnessing sulfinyl nitrenes: A unified one-pot synthesis of sulfoximines and sulfonimidamides", Thomas Q. Davies, Michael J. Tilby, Jack Ren, Nicholas A. Parker, David Skolc, Adrian Hall, Fernanda Duarte,and Michael C. Willis, J. Am. Chem. Soc. 2020, 142, 15445−15453. (doi: 10.1021/jacs.0c06986)

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152 ga

 

“alpha-Amidoaldehydes as substrates in rhodium-catalyzed intermolecular alkyne hydroacylation: The synthesis of alpha-amidoketones”, Ritashree Pal, Sean C. O'Brien and Michael C. Willis, Chem. Eur. J202026, 11710-11714. (doi: 10.1002/chem.202002478).

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151 ga

 

“Mechanism of the month: Palladium-catalyzed desulfinative cross-couplings”, Antoine de Gombert and Michael C. Willis, Trends in Chemistry 20202, 865-866. (doi: 10.1016/j.trechm.2020.04.004)

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150 ga

 

"Hydrosulfonylation of alkenes with sulfonyl chlorides under visible light activation”, Sandrine Monique Hell, Claudio Flavio Meyer, Antonio Misale, Jeroen B. I. Sap, Kirsten K. Christensen, Michael C. Willis, Andrés A. Trabanco, and Veronique Gouverneur,* Angew. Chem. Int. Ed. 202059, 11620-11626. (doi: 10.1002/anie.202004070)

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149 ga 40

 

“Sulfinamide Synthesis using Organometallic reagents, DABSO and Amines”, Pui Kin Tony Lo, Gwyndaf A. Oliver, Michael C. Willis, J. Org. Chem202085. 5753-5760. (doi: 10.1021/acs.joc.0c00334)

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148 ga 35

 

“Mechanistic studies of the palladium-catalyzed desulfinative cross-coupling of aryl bromides and (hetero)aryl sulfinate salts “, Antoine de Gombert, Alasdair I. McKay, Christopher Davis, Katherine M. Wheelhouse, and Michael C. Willis, J. Am. Chem. Soc2020142, 3564-3576. (doi: 10.1021/jacs.9b13260).

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graphical abstract40

 

“Silyl radical-mediated activation of sulfamoyl chlorides enables direct access to aliphatic sulfonamides from alkenes”, Sandrine M. Hell, Claudio F. Meyer, Gabriele Laudadio, Antonio Misale, Michael C. Willis, Timothy Noël, Andrés A. Trabanco, and Véronique Gouverneur,* J. Am. Chem. Soc2020142, 720−725. (doi: 10.1021/jacs.9b13071)

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145 ga 20

 

18F-Trifluoromethanesulfinate enables direct C–H 18F-trifluoromethylation of native aromatic residues in peptides”, Choon Wee Kee, Osman Tack, Florian Guibbal, Patrick G. Isenegger, Thomas C. Wilson, Mateusz Imiołek, Stefan Verhoog, Michael Tilby, Giulia Boscutti, Sharon Ashworth, Juliette Chupin, Roxana Kashani,  Adeline W. J. Poh, Jane K. Sosabowski, Sven Macholl,  Christophe Plisson, Bart Cornelissen, Michael C. Willis, Jan Passchier, Benjamin G. Davis, Véronique Gouverneur,* J. Am. Chem. Soc2020142, 1180−1185. (doi: 10.1021/jacs.9b11709)

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146 ga 40

 

“Synthesis of highly fluorinated arene complexes of [Rh(chelating phosphine) cations, and their use in synthesis and catalysis”, Alasdair I. McKay, James Barwick-Silk, Max Savage, Michael C. Willis and Andrew S. Weller,* Chem. Eur. J202026, 2883-2889. (doi: 10.1002/chem.201904668).

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