Abstract

Cyclohexa-2,4-dienones stabilized by coordination to tricarbonyliron are obtained when tosylhydrazones of tricarbonyliron complexed dienones are submitted to the conditions of the Bamford-Stevens reaction (thermolysis in the presence of strong bases). This cyclocarbonylation reaction proceeds most likely via α-diazodiene complexes, and from there via carbenes, which react intramolecularly with a CO ligand, the coordinatively unsaturated iron species so formed being finally stabilized by an external two-electron ligand. The existence of two such hypothetical intermediates could be proven by intramolecular trapping experiments (1,3-dipolar cycloadducts 3, ansa Fe(CO) 2 complex 6, structures confirmed by X-ray diffraction).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.