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Amido-Grignard

Use of Amido Grignard Reagents in Inorganic Chemistry—Synthesis and Crystal Structure of Anti (Ragaini et al., 1997)... [Pg.188]

Imidazolium ligands, in Rh complexes, 7, 126 Imidazolium salts iridium binding, 7, 349 in silver(I) carbene synthesis, 2, 206 Imidazol-2-ylidene carbenes, with tungsten carbonyls, 5, 678 (Imidazol-2-ylidene)gold(I) complexes, preparation, 2, 289 Imidazopyridine, in trinuclear Ru and Os clusters, 6, 727 Imidazo[l,2-a]-pyridines, iodo-substituted, in Grignard reagent preparation, 9, 37—38 Imido alkyl complexes, with tantalum, 5, 118—120 Imido-amido half-sandwich compounds, with tantalum, 5,183 /13-Imido clusters, with trinuclear Ru clusters, 6, 733 Imido complexes with bis-Gp Ti, 4, 579 with monoalkyl Ti(IV), 4, 336 with mono-Gp Ti(IV), 4, 419 with Ru half-sandwiches, 6, 519—520 with tantalum, 5, 110 with titanium(IV) dialkyls, 4, 352 with titanocenes, 4, 566 with tungsten... [Pg.125]

Perfluoroalkyl- and perfluoroaryltitanium compounds were prepared m situ via reaction of the corresponding Grignard reagents with chlorotris(diethyl-amido)titaniuin [2SS] Reaction of the titanium compounds with aldehydes resulted in fluoroalkylative amination [2SS] (equation 192)... [Pg.718]

Schultz and Harrington [37] added Grignards to a-amido enone (see Table 4, entry 6). They obtained high diasteromeric excesses with a variety of nucleophiles for example, with methyl Grignard reagent, the d.e. ranged from 85 to 90%. [Pg.567]

These 0x0 Re complexes can furnish various derivatives, for example, with N-, 0-, S-, or C- ligands, that is, Re oxo-amido, -imido, -alkoxide, -phenoxide, -diolate, -thiolate, -alkyl, or - aryl complexes, on reactions of (13) or (14) with amines, alcohols, phenoxides, diols, thiols, organozinc, or Grignard reagents, respectively. [Pg.4762]

Reduction of an alkylmercury halide or acetate with a borohydride provides an alternative method for accessing a carbon radical species (see Scheme 4.11). The alkylmercury compound can be prepared by one of a number of methods, such as from the corresponding Grignard reagent or from addition of Hg(OAc)2 to an alkene. For example, intramolecular amido-mercurafion of the alkene 50, followed by formation of the alkyl radical and addition to methyl acrylate provides a route to the alkaloid 8-coniceine (4.46). ... [Pg.285]


See other pages where Amido-Grignard is mentioned: [Pg.207]    [Pg.421]    [Pg.219]    [Pg.5351]    [Pg.5350]    [Pg.207]    [Pg.421]    [Pg.219]    [Pg.5351]    [Pg.5350]    [Pg.44]    [Pg.627]    [Pg.112]    [Pg.319]    [Pg.109]    [Pg.129]    [Pg.130]    [Pg.109]    [Pg.129]    [Pg.130]    [Pg.653]    [Pg.422]    [Pg.39]    [Pg.61]    [Pg.163]    [Pg.154]    [Pg.103]    [Pg.86]    [Pg.794]    [Pg.4763]    [Pg.582]    [Pg.109]    [Pg.129]    [Pg.130]    [Pg.443]    [Pg.429]    [Pg.330]    [Pg.343]    [Pg.348]    [Pg.351]    [Pg.457]    [Pg.169]    [Pg.90]    [Pg.86]    [Pg.793]    [Pg.188]    [Pg.55]    [Pg.58]   
See also in sourсe #XX -- [ Pg.207 ]




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