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Methylenecyclopropane iron tetracarbonyl

First, cis- and trans-2-phenylmethylenecyclopropanes-3-d were shown to give trimethyl-enemethane complexes with the deuterium at a location consistent only with disrotatory ring-opening (Figure 41). Second, reaction of 2,2-diphenylmethylenecyclopropane with a variety of iron carbonyl reagents allowed isolation of the methylenecyclopropane iron tetracarbonyl complex. This compound could be shown to give the trimethylenemethane complex on reaction with trimethylamine-N-oxide or diiron nonacarbonyl, both of which... [Pg.1059]


See other pages where Methylenecyclopropane iron tetracarbonyl is mentioned: [Pg.1059]    [Pg.1060]    [Pg.1059]    [Pg.1060]    [Pg.624]    [Pg.624]    [Pg.634]    [Pg.636]    [Pg.634]    [Pg.636]   


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Methylenecyclopropane iron tetracarbonyl complex

Methylenecyclopropanes

Tetracarbonyl iron

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