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Silane methoxytrimethyl

C4H 2OSi, Silane, methoxytrimethyl-, 26 44 CH4N, Propane, 2-isocyant-2-methyl-ruthenium complex, 26 275 C][l,4]-dithiin-2-thione, 26 389 CHfc, 1,3-Cyclopentadiene cobalt complex, 26 191-197, 309 chromium, molybdenum, and tungsten complexes, 26 343 iron complex, 26 232-241 mercury-molybdenum-ruthenium complex, 26 333... [Pg.414]

SiOCjH, Silane, methoxytrimethyl-, 26 44 Si3Ci4H , Benzene, 1,2-bis[(trimethylsilyl)-methyl]-, 26 148... [Pg.443]

OPSi2C,H27, Phosphine, [2,2-dimethyl-1-(trimethylsiloxy)propylidene](tri-methylsilyl)-, 27 250 OS2CH, Dithiocarbonic acid, 27 287 OSiC4H 2, Silane, methoxytrimethyl-,... [Pg.403]

SiOC4H,2, Silane, methoxytrimethyl-, 26 44 SiPC2iH39, Phosphine, (2,4,6-tri-tert-batylphenyQ(trimethylsilylK 21 23% Si2Br2UC22H42. Uranium(IVX bis(9 -13-bis(triniethylsflyl)cydopentadienyl]di-bromo-, 27 174... [Pg.458]

Trimethylsilylmethylenephosphoranes have two different electrophilic sites (P, Si). Reaction of these species with methanol generates methoxytrimethyl-silane and methylenephosphoranes (51). Apparently silicon is a harder acceptor than tetrahedral phosphorus. [Pg.170]

See other pages where Silane methoxytrimethyl is mentioned: [Pg.158]    [Pg.429]    [Pg.377]    [Pg.428]    [Pg.41]    [Pg.349]    [Pg.377]    [Pg.428]    [Pg.392]    [Pg.429]    [Pg.392]    [Pg.158]    [Pg.429]    [Pg.377]    [Pg.428]    [Pg.41]    [Pg.349]    [Pg.377]    [Pg.428]    [Pg.392]    [Pg.429]    [Pg.392]    [Pg.27]    [Pg.183]    [Pg.290]    [Pg.954]    [Pg.420]   
See also in sourсe #XX -- [ Pg.26 , Pg.44 ]

See also in sourсe #XX -- [ Pg.26 , Pg.44 ]



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