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Organoantimony hydrides

The most frequently used synthetic procednre for organoantimony hydrides is the reaction of an organoantimony... [Pg.220]

Other methods of organoantimony hydride synthesis are reactions of R2SbLi with (Me3NH)Cl or methanolysis of silylstibines RSb(SiMc3)2 or R2SbSiMc3. Vinyl stibine H2C=C(H)-SbH2 is obtained from vinyl tributylstaimane on successive reactions (equation 8) with SbCb and BusSnH. ... [Pg.221]

Organoantimony and -bismuth(III) halides are reduced with hydride reagents at low temperatures (equations 61 , 62 , 63 and 64 °). [Pg.773]

See other pages where Organoantimony hydrides is mentioned: [Pg.220]    [Pg.220]    [Pg.219]    [Pg.219]    [Pg.220]    [Pg.220]    [Pg.219]    [Pg.219]    [Pg.761]    [Pg.761]    [Pg.773]    [Pg.534]    [Pg.544]    [Pg.58]   
See also in sourсe #XX -- [ Pg.317 , Pg.318 ]

See also in sourсe #XX -- [ Pg.317 , Pg.318 ]



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