Abstract
Without suffering from β-elimination, cobalt complexes allow cross-coupling reactions of alkyl halides with Grignard reagents. A combination of a cobalt complex and trimethylsilylmethyl Grignard reagent effects Mizoroki-Heck-type reaction of alkyl halide with styrene, which conventional palladium catalysts have never made possible. Cobalt exhibits intriguing catalytic activities on hydrophosphination and allylzincation of alkynes. Silylmethylcobalt reagent is a powerful tool for the synthesis of highly silylated ethenes. © 2006 IUPAC.
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Yorimitsu, H., & Oshima, K. (2006). New synthetic reactions catalyzed by cobalt complexes. In Pure and Applied Chemistry (Vol. 78, pp. 441–449). https://doi.org/10.1351/pac200678020441
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