Issue 2, 1992

Synthesis of tricarbonyl(vinylallene)iron(0) complexes from tricarbonyl(vinylketene)iron(0) complexes and their oxidation to 5,5-disubstituted furan-2(5H)-ones

Abstract

Addition of phosphonoacetate anions to tricarbonyl(vinylketene)iron(0) complexes gave tricarbonyl(vinylallene)iron(0) complexes. Stereoselectivity as high as 98 : 2 was observed and the relative stereochemistry of the major stereoisomers was elucidated by X-ray crystal structure analysis of the major isomer of [Feo{PhCH[double bond, length half m-dash]CHC(Me)[double bond, length half m-dash]C[double bond, length half m-dash]CHCO2But}(CO)3]9d, the product obtained from the reaction between [Feo{PhCH[double bond, length half m-dash]CHC(Me)[double bond, length half m-dash]C[double bond, length half m-dash]O}(CO)3]7a and the anion of (EtO)2 P(O)CH2CO2But8b. Reaction of the major isomers of the tricarbonyl(vinylallene)iron(0) complexes with FeCl3 gave 5,5-disubstituted furan-2(5H)-ones.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 259-265

Synthesis of tricarbonyl(vinylallene)iron(0) complexes from tricarbonyl(vinylketene)iron(0) complexes and their oxidation to 5,5-disubstituted furan-2(5H)-ones

S. P. Saberi and S. E. Thomas, J. Chem. Soc., Perkin Trans. 1, 1992, 259 DOI: 10.1039/P19920000259

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