Issue 7, 1974

The stereochemistry of electrophilic addition to tricarbonyldieneiron complexes

Abstract

The X-ray structural analysis of a substituted tricarbonylallyliron cationic intermediate unambiguously demonstrates that tricarbonyl(trans, trans-hexa-2,4-diene)iron undergoes stereospecific endo attack under Friedel-Crafts conditions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 257-258

The stereochemistry of electrophilic addition to tricarbonyldieneiron complexes

E. O. Greaves, G. R. Knox, P. L. Pauson, S. Toma, G. A. Sim and D. I. Woodhouse, J. Chem. Soc., Chem. Commun., 1974, 257 DOI: 10.1039/C39740000257

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