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Phosphino silane

The use of the phosphinoaluminate reagent Li[Al(PH2)4] has found application in the synthesis of a family of organotris(phosphino)silanes (27).37... [Pg.258]

Figure 3.89 Syntheses of a phosphino functionalised imidazolium salt using the silane reduction route. Figure 3.89 Syntheses of a phosphino functionalised imidazolium salt using the silane reduction route.
Phosphane 9 is a useful intermediate which can be converted easily into trifluoromethyl anion equivalents, e. g. trimclhyl(trifluoromethyl)silane. Similarly, 1,2-bis(dichlorophosphi-iio)cthanc (10) and bromotrifluoromclhane react in the presence of 8 to form l,2-bis[bis(tri-fluoromethyl)phosphino]ethane (11). ... [Pg.667]

See other pages where Phosphino silane is mentioned: [Pg.182]    [Pg.3]    [Pg.466]    [Pg.231]    [Pg.151]    [Pg.168]    [Pg.3]    [Pg.13]    [Pg.84]    [Pg.84]    [Pg.182]    [Pg.3]    [Pg.466]    [Pg.231]    [Pg.151]    [Pg.168]    [Pg.3]    [Pg.13]    [Pg.84]    [Pg.84]    [Pg.215]    [Pg.2064]    [Pg.685]    [Pg.3728]    [Pg.3918]    [Pg.17]    [Pg.24]    [Pg.6]    [Pg.588]    [Pg.3727]    [Pg.3917]    [Pg.7]    [Pg.65]    [Pg.9]    [Pg.151]    [Pg.169]    [Pg.3]    [Pg.28]    [Pg.102]    [Pg.2064]    [Pg.979]    [Pg.2591]    [Pg.9]    [Pg.9]   
See also in sourсe #XX -- [ Pg.466 , Pg.484 ]



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