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01056 am a22001813u 4500 |
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141143 |
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|a dc
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|a Leypold, Mario
|e author
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|a D'Angelo, Kyan A
|e author
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|a Movassaghi, Mohammad
|e author
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|a Chemoselective α-Sulfidation of Amides Using Sulfoxide Reagents
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|b American Chemical Society (ACS),
|c 2022-03-10T20:13:13Z.
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| 856 |
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|z Get fulltext
|u https://hdl.handle.net/1721.1/141143
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|a © 2020 American Chemical Society The direct α-sulfidation of tertiary amides using sulfoxide reagents under electrophilic amide activation conditions is described. Employing convenient and readily available reagents, selective functionalization takes place to generate isolable sulfonium ions en route to α-sulfide amides. Mechanistic studies identified activated sulfoxides as promoters of the desired transformation and enabled the extension of the methodology from benzylic to aliphatic amide substrates.
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| 546 |
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|a en
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|a Article
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| 773 |
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|t 10.1021/ACS.ORGLETT.0C03160
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| 773 |
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|t Organic Letters
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