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Stannyls organo

Lithium alkanetellurolates, prepared from tellurium and an alkyl lithium compound or dialkyl ditellurium derivatives and hthium, and sodium arenetellurolates, obtained from diaryl ditellurium compounds and sodium borohydride ", reacted with triorganosilyl, -germyl, -stannyl, and -plumbyl chlorides to produce, for instance, organo triorganosilyl tellurium compounds. [Pg.187]

Organo-silanes and -stannanes possessing sp caibon-metal bonds also add to carbonyls in the presence of Lewis acids. Alkynylation with silyl- and stannyl-alkynes is promoted by AlCb or Z11CI2 (equations 9 and lO). " Notably, the reaction of l,3-bis(trimethylsilyl)-l-prcq>yne with chloral affords ynic alcohol instead of allenylic alcohol, showing the preferential cleavage of sp C—Si bonds (equation 11). ... [Pg.328]

H. Schumann, Organo germyl, stannyl and plnmbyl phosphines, AWC, 8, 937, 1969. [Pg.821]

Stannyl hydrides s. Tin hydrides, organo-Stark s. Dean Statistics, mathematical, optimization by - 13, 696 suppl. 27 Stereodiemistry... [Pg.310]

See other pages where Stannyls organo is mentioned: [Pg.89]    [Pg.607]    [Pg.293]    [Pg.89]    [Pg.89]    [Pg.335]    [Pg.187]    [Pg.470]    [Pg.89]    [Pg.470]    [Pg.322]    [Pg.167]    [Pg.372]    [Pg.382]    [Pg.328]    [Pg.197]    [Pg.380]    [Pg.278]   


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