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Imino-phosphine complexes

Other catalytic systems were used recently, namely a Ddppi system (67, Scheme 8.14) for dicyclopentadiene and di(methylcyclopentadiene) [96] and imino-phosphine complexes (Scheme 8.19, 97 and 98) or hybrid terdentate carbene hgand complexes (99) [133] for norbornene. Furtlierrnore, the copolymerization of various substituted norbomadienes and norbomenes has been achieved with Rh6(CO)i6 under water gas shift reaction conditions (55 ""C, water and 100 atm CO) [134],... [Pg.298]

Wirringa et al. obtained an unusual l,3-diaza-2-phosphaallyl(methylzinc) complex (Figure 44, 85), featuring a two-coordinate phosphorus atom, from the deprotonation of a bulky amino(imino)phosphine with dimethylzinc.144... [Pg.354]

Ferraris et al.108 demonstrated an asymmetric Mannich-type reaction using chiral late-transition metal phosphine complexes as the catalyst. As shown in Scheme 3-59, the enantioselective addition of enol silyl ether to a-imino esters proceeds at —80°C, providing the product with moderate yield but very high enantioselectivity (over 99%). [Pg.185]

Lectka and co-workers found that cationic Cu phosphine complexes are efficient Lewis acids in the activation of a-imino esters (248). The Tol-BINAP was found to be the most effective ligand providing the adduct of acetophenone enol-... [Pg.129]

The cationic Pd(II)-7i-allyl complexes of the formula [(Ligand)Pd(ri3-C3H5)]PF6 (Ligand = ferrocenyl imino-phosphine la-e) were isolated in the solid state by the literature procedure15,61 using [(ri3-C3H5)PdCl]2 as starting material.[7] The complexes obtained were used as catalyst precursors for the asymmetric allylic... [Pg.55]

Thus, organosilicon hydrides can serve as reducing agents like metal hydrides so far as the catalytic hydrosilylation is effectively achieved. To date, rhodium(I)-phosphine complexes have been found to be by far the most useful catalysts for these purposes, especially for the asymmetric reduction of carbonyl and imino compounds. [Pg.189]

Multiple, successive insertion of isonitriles into the palladium-carbon o--bond has also been found with organopalladium(II)bis(phosphine) complexes. However, unlike the Ni- catalyzed polymerization, only single, double, and triple insertion reactions of isonitriles have been reported for Pd-mediated reactions. For instance, reaction of methylpalladium(II) complex 2 with cyclohexyl isonitrile in ratios of 1 1, 1 2, and 1 3 afforded selectively single (3), double (4), and triple (5) insertion products, respectively (Scheme 3). However, no further insertion of cyclohexyl isonitrile to 5 took place. No reactivity of the triple insertion complex 5 was explained by the intramolecular coordination of the nitrogen atom of the third imino group, which formed a stable five-mem-bered chelating palladium complex. [Pg.1045]

Single-photon emission computed tomography Tricarbonyltris(2-methoxyisobutyl isonitrile)99mTc complex Hexakis(2-ethoxy-isobutylisonitrile)99mTc complex trans[(l,2-Bis(dihydro-2,2,5,5-tetramethyl-3(2H)furanone-4-methylene-imino)ethane) bis(tris(3-methoxy-l-propyl)phosphine)]99mTc complex Hexakis(2-methoxyisobutyl isonitrile)"mTc complex [l,2-Bis bis(2-ethoxyethyl)phosphino ethane]20299mTc complex... [Pg.156]

Adenosine triphosphate alkali metal complexes, 34 vanadyl complexes, 568 Alane, 123 amine adducts, 107 phosphine adducts, 111 Alane, alkoxy-, 124 Alane, amino-, 109 Alane, imino-, 109 Alkali metal complexes, 1-70 acid anions, 30 acid salts, 30 bipyridyl, 13 crown ethers cavity size, 38 cryptates... [Pg.3286]


See other pages where Imino-phosphine complexes is mentioned: [Pg.443]    [Pg.55]    [Pg.71]    [Pg.32]    [Pg.186]    [Pg.51]    [Pg.489]    [Pg.277]    [Pg.231]    [Pg.467]    [Pg.465]    [Pg.485]    [Pg.117]    [Pg.304]    [Pg.71]    [Pg.29]    [Pg.119]    [Pg.312]    [Pg.326]    [Pg.637]    [Pg.377]    [Pg.581]    [Pg.147]    [Pg.341]    [Pg.581]    [Pg.233]    [Pg.269]    [Pg.250]    [Pg.327]    [Pg.62]    [Pg.69]    [Pg.93]    [Pg.5510]    [Pg.268]   
See also in sourсe #XX -- [ Pg.298 ]




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Imino complexes

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