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Organovanadium reagents

Organocopper reagents, 207 Organomanganese(II) iodides, 210 Organotin reagents, 211 Organovanadium reagents, 219... [Pg.353]

Organocopper reagents, 207 Organovanadium reagents, 219 By desilylation of vinylsilanes Tetrabutylammonium fluoride, 286 By desulfurization of vinyl sulfides and related sulfur compounds Sodium dithionite, 281 Elimination reactions By dehalogenation Dichlorobis(cyclopentadienyl)-titanium, 102... [Pg.382]

Organomanganese(II) iodides, 210 Organotin reagents, 211 Organovanadium reagents, 219 From carboxylic acids Benzylchlorobis(triphenylphos-phine)palladium(II), 30 From other acyl derivatives Lithium o-lithiophenoxide, 166 Organomanganese(II) iodides, 210 From 1,2-diols or 1,2-amino alcohols Diethoxy triphenylphosphorane, 109... [Pg.393]

Organovanadium reagents, 219 Phenylmagnesium bromide-Vanadi-um(III) chloride, 219 Vanadium(III) chloride, 219 Vanadyl acetylacetonate, 54 Vanadyl trichloride, 289 Zinc Compounds Bis(acetylacetonate)zinc(II), 33... [Pg.415]

Organovanadium reagents have been used to effect two useful... [Pg.410]

The investigation on the chemistry of organovanadium compounds is rather limited probably because of the difficulty in the characterization and isolation, but their properties and reactivities appear to be of potential as materials, medicine, reagents, and catalysts. Functionalization or design of organic moieties and redox properties will provide a variety of organovanadium compounds, which may open the door of new vanadium chemistry. [Pg.5056]

See other pages where Organovanadium reagents is mentioned: [Pg.362]    [Pg.362]    [Pg.366]    [Pg.49]    [Pg.240]    [Pg.362]    [Pg.362]    [Pg.366]    [Pg.49]    [Pg.240]    [Pg.5040]    [Pg.5052]    [Pg.33]    [Pg.5039]    [Pg.5051]   
See also in sourсe #XX -- [ Pg.219 ]

See also in sourсe #XX -- [ Pg.219 ]

See also in sourсe #XX -- [ Pg.240 ]



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