Further evidence for the FeII-FeIV and FeIII-FeV manifolds in the substitution of saturated hydrocarbons
β Scribed by Derek H.R. Barton; Beatrice M. Chabot; Nathalie C. Delanghe; Bin Hu; Valerie N. Le Gloahec; Roy U. Rojas Wahl
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 227 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
In the Fem-Fe v manifold the formation of the iron-carbon bond was found to be very fast, but the evolution to give ketone was slow at -20 \*C and -40 \*C. However, the efficiency at the latter temperature was good. The iron-carbon bond can be captured rapidly by I" or by PhSeH. We have confirmed th
Competition experiments between cyclohexane and various aromatic substrates have been carried out in pyridine-acetonitrile in order to ascertain the steric requirements of the FeI~-H202 reagent in comparison with the Fem-H202 reagent already studied. The latter is distinctly larger and much less rea
The selective functionalization of alkane was achieved in a good yield. by a simple Fe"Clz salt and bis(trimethylsily1) peroxide in pyridine. Unlike the Fen-HZ02 system, no extra ligand was needed. The presence of a carbon radical from the Fen-Few manifold was proposed to explain the results.