Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbon±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 ±sp, sp 2 ±sp 2 , a
Cobalt-Catalyzed Coupling Reaction of Alkyl Halides with Allylic Grignard Reagents.
✍ Scribed by Takashi Tsuji; Hideki Yorimitsu; Koichiro Oshima
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 229 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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Nickel-and palladium-catalyzed cross-coupling reactions of organic halides with organometallic reagents is one of the most versatile carbon±carbon bond-forming reactions in organic synthesis. [1] In most cases, aryl and vinyl halides are employed as organic halides, yielding sp 2 ±sp, sp 2 ±sp 2 , a
## Abstract Details of cobalt‐catalyzed cross‐coupling reactions of alkyl halides with allylic Grignard reagents are disclosed. A combination of cobalt(II) chloride and 1,2‐bis(diphenylphosphino)ethane (DPPE) or 1,3‐bis(diphenylphosphino)propane (DPPP) is suitable as a precatalyst and allows second