Cover Feature: Diarylcuprates for Selective Syntheses of Multifunctionalized Ketones from Thioesters under Mild Conditions (Chem. Eur. J. 26/2022)
The synthesis of ketone as a synthetic intermediate of canagliflozin from a gluconolactone‐derived thioester and a Grignard reagent with the aid of copper is likened to making Taiyaki, a Japanese fish‐shaped waffle with sweet red bean inside. The thioester (sweet red beans) and the Grignard reagent...
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Veröffentlicht in: | Chemistry : a European journal 2022-05, Vol.28 (26), p.n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The synthesis of ketone as a synthetic intermediate of canagliflozin from a gluconolactone‐derived thioester and a Grignard reagent with the aid of copper is likened to making Taiyaki, a Japanese fish‐shaped waffle with sweet red bean inside. The thioester (sweet red beans) and the Grignard reagent (waffle batter) are baked on a copper waffle iron to get the desired ketone as Taiyaki. More information can be found in the Research Article by H. Tsurugi, M. Seki, K. Mashima, and co‐workers (DOI: 10.1002/chem.202200474). |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.202201013 |