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Triisopropylphosphine

COi is another molecule which reacts with conjugated dienes[10,95,96], COt undergoes cyclization with butadiene to give the five- and six-membered lactones 101. 102. and 103, accompanied by the carboxylic esters 104 and 105[97.98], Alkylphosphines such as tricyclohcxyl- and triisopropylphosphine are recommended as ligands. MeCN is a good solvent[99],... [Pg.439]

The delta lactone can be obtained in very high yields when triisopropylphosphine or tricyclohexylphosphine is the ligand along with Pd(acac)2 as the metal source (171). [Pg.345]

Alkyl lithiums Dodecacarbonyltetracobalt Barium sulphide Triisopropylphosphine... [Pg.189]

Complexes of triisopropylphosphine (cone angle 160°) [69, 117]. In contrast to less bulky trialkylphosphines, a complex RhCl3(PPr3)3 has only been made by reaction at 0°C at higher temperatures, hydrides like RhHCl2(PPr 3)2 result (the less bulky tri(n-propyl)phosphine gives the 3 1 complex at reflux). [Pg.130]

Reaction of RhCl3 and sodium amalgam with triisopropylphosphine under a hydrogen atmosphere yields a distorted square planar complex RhH(PPr3)3 (Figure 2.66). [Pg.130]

Figure 2.64 Interrelationships between rhodium complexes of triisopropylphosphine. Figure 2.64 Interrelationships between rhodium complexes of triisopropylphosphine.
Palladium, (diammine)bis(thiocyanato)-isomerism, 1, 185 Palladium, dichlorobis(amine)-substitution reactions stereochemistry, 1, 318 Palladium, dichlorobis(pyridine)-substitution reactions, 1, 314 Palladium, dinitritobis(triisopropylphosphine)-substitution reactions, I, 314 Palladium, ethylene-synthesis... [Pg.188]

Esteruelas, Miguel A. The Chemical and Catalytic Reactions of Hydrido-chloro-carbonylbis (triisopropylphosphine) osmium and... [Pg.466]

The interaction of triisopropylphosphine with chloroform is extremely violent, if in the absence of solvent. [Pg.274]

In 1979, the first isolation of the hydrido(hydroxo) complex by oxidative addition of water to an electron-rich platinum(O) complex was accomplished by Yoshida and Otsuka [22]. Highly coordinatively unsaturated bis(triisopropylphosphine)platinum (24b) can activate water very easily at room temperature to give the hydrido(hydroxo)... [Pg.175]


See other pages where Triisopropylphosphine is mentioned: [Pg.1019]    [Pg.372]    [Pg.391]    [Pg.229]    [Pg.315]    [Pg.3]    [Pg.3]    [Pg.4]    [Pg.5]    [Pg.7]    [Pg.9]    [Pg.11]    [Pg.13]    [Pg.15]    [Pg.17]    [Pg.19]    [Pg.21]    [Pg.23]    [Pg.25]    [Pg.27]    [Pg.29]    [Pg.31]    [Pg.33]    [Pg.35]    [Pg.37]    [Pg.39]    [Pg.41]    [Pg.43]    [Pg.44]    [Pg.45]    [Pg.47]    [Pg.49]    [Pg.51]    [Pg.53]    [Pg.55]    [Pg.57]    [Pg.59]   
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See also in sourсe #XX -- [ Pg.14 ]

See also in sourсe #XX -- [ Pg.432 ]

See also in sourсe #XX -- [ Pg.244 ]

See also in sourсe #XX -- [ Pg.432 ]

See also in sourсe #XX -- [ Pg.78 ]




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Complexes of triisopropylphosphine

Dihydrido Arene Iridium Triisopropylphosphine Complexes

Dihydrido Iridium Triisopropylphosphine Complexes From Organometallic Chemistry to Catalysis

Dihydrido Iridium Triisopropylphosphine Complexes as Imine Hydrogenation Catalysts

Tris(triisopropylphosphine)platinum

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