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Fe-Catalyzed Cross-Coupling of Alkyl Halides with Alkynyl Grignard Reagents
| Content Provider | Semantic Scholar |
|---|---|
| Author | Knochel, Paul Steib, Andreas K. |
| Copyright Year | 2012 |
| Abstract | Significance: The authors report a novel coupling of primary and secondary alkyl halides with alkynylmagnesium reagents with iron catalysis. The use of a bisphosphine ligand bearing peripheral steric bulk as well as slow addition of the Grignard reagent suppress undesired side reactions. Comment: By using starting materials with two potential reactive sites, for example C(sp3)–Br and C(sp2)–OTf, and applying the reported ironcatalyzed cross-coupling with an alkynyl Grignard reagent, the C(sp)–C(sp3)-coupled products are obtained in excellent yields. Alkyl X BrMg R catalyst (3–5 mol%) THF, 60 °C, 2–4 h + Alkyl R |
| Starting Page | 193 |
| Ending Page | 193 |
| Page Count | 1 |
| File Format | PDF HTM / HTML |
| DOI | 10.1055/s-0031-1290007 |
| Volume Number | 8 |
| Alternate Webpage(s) | https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0031-1290007.pdf |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |