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Cyclooctatetraeneiron tricarbonyl

The mass spectrum of cyclooctatetraeneiron tricarbonyl shows stepwise loss of the three carbonyl groups from the molecular ion, followed by elimination of acetylene giving C6H6Fe+, and further breakdown gives Fe+ (119). The mass spectra of two substituted cyclooctatetraene complexes (see Table VIII) show the molecular ion and stepwise loss of the carbonyl groups (83). [Pg.269]

M. D. Rausch, and G. N. Schrauzer, Cyclooctatetraeneiron Tricarbonyl and Cycloocta-tetraenediiron Hexacarbonyl, Chem. Ind. 1959, 957-958. [Pg.231]

Cycloaddition (5,647-648). The first step in a synthesis of (+)-2,3-dihydro-triquinacenone-2 (5) involves addition of TCNE to cyclooctatetraeneiron tricarbonyl (1) in a 1,3-bonding scheme. The yield is surprisingly high (96%). The iron atom is then extruded by oxidation with ceric ammonium nitrate (4, 72)... [Pg.567]

Cyclooctadiene-1,5, 23, 62, 445 Cyclooctane-1,2-diol, 384 Cyclooctane-1,5-diol, 64 Cyclooctanol, 183 Cyclooctatetraene, 23 Cyclooctatetraene epoxide, 306, 519 Cyclooctatetraeneiron tricarbonyl, 567 Cyclooctene, 23, 183, 445 Cyclooctene oxide, 334 Cyclooctyl fluoride, 183 Cyclopentadiene, 123, 291 Cyclopentadienone, 454 iT-CycIopentadienylcobalt dicarbonyl, 153-154... [Pg.371]


See other pages where Cyclooctatetraeneiron tricarbonyl is mentioned: [Pg.231]    [Pg.120]    [Pg.66]    [Pg.231]    [Pg.120]    [Pg.66]   
See also in sourсe #XX -- [ Pg.567 ]




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