## Abstract After quenching with an electrophile, the resulting sulfoxide is converted into a second magnesium reagent with iPrMgCl·LiCl (sulfoxide—magnesium exchange), which can be trapped with various electrophiles.
ChemInform Abstract: Difunctionalization of Arenes and Heteroarenes by Directed Metallation and Sulfoxide—Magnesium Exchange.
✍ Scribed by Laurin Melzig; Christian B. Rauhut; Nikolaus Naredi-Rainer; Paul Knochel
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 66 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
Highly functionalized 1,2,4‐trisubstituted arenes and difunctionalized heteroarenes (furans, thiophenes, benzofurans and pyridines) are prepared in a two‐step sequence using the sulfoxide moiety.
📜 SIMILAR VOLUMES
Scheme 1. Metallation of sulfoxides, followed by a sulfoxide-magnesium exchange reaction, leading to 1,2,4-trifunctionalised arenes.
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