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- W2893361790 abstract "Alkene aminoarylation with a single, bifunctional reagent is a concise synthetic strategy. We report a catalytic protocol for the addition of arylsulfonylacetamides across electron-rich alkenes with complete anti-Markovnikov regioselectivity and excellent diastereoselectivity to provide 2,2-diarylethylamines. In this process, single-electron alkene oxidation enables carbon-nitrogen bond formation to provide a key benzylic radical poised for a Smiles-Truce 1,5-aryl shift. This reaction is redox-neutral, exhibits broad functional group compatibility, and occurs at room temperature with loss of sulfur dioxide. As this process is driven by visible light, uses readily available starting materials, and demonstrates convergent synthesis, it is well suited for use in a variety of synthetic endeavors." @default.
- W2893361790 created "2018-10-05" @default.
- W2893361790 creator A5036992723 @default.
- W2893361790 creator A5051000767 @default.
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- W2893361790 date "2018-09-28" @default.
- W2893361790 modified "2023-10-11" @default.
- W2893361790 title "Arylsulfonylacetamides as bifunctional reagents for alkene aminoarylation" @default.
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- W2893361790 doi "https://doi.org/10.1126/science.aat2117" @default.
- W2893361790 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30262501" @default.
- W2893361790 hasPublicationYear "2018" @default.
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