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Rh-dppf

The Rh-catalyzed hydroacylation of alkynes is also possible. Reaction of salicyl-aldehyde (611) with 4-octyne using an Rh-DPPF complex gave the unsaturated ketone 612 in high yield [236],... [Pg.295]

Square planar cis-[Rh(dppf-P, P)(nbd)l[C10J chelate gauche (staggered) ... [Pg.20]

The temperature-dependent P NMR spectrum of [Rh(dppf-P,P )2][BPh4] reveals a different kind of solution fluxionality [65], which invokes changes in both... [Pg.43]

Fig. 1-20. 162 MHz NMR spectrum of [Rh(dppf-P, F)2][BPh4] at 183 K showing an A2M2X spin pattern (adapted from [65]). Fig. 1-20. 162 MHz NMR spectrum of [Rh(dppf-P, F)2][BPh4] at 183 K showing an A2M2X spin pattern (adapted from [65]).
More recentiy, a rhodium-catalyzed carbonylation of arylzinc compounds was developed by Takagi [117]. In the presence of an Rh-dppf catalyst under 1 bar of CO using 1,2-dibromoethane as the oxidant, carbonylative homo-coupling of arylzinc compounds was achieved, affording symmetrical diaryl ketones in good yields (Scheme 8.33). Under similar conditions, Pd or Ni catalysts induced oxidative homo-coupling of zinc reagents to yield diaryls instead. [Pg.162]

Cobalt and Rhodium The molecular structure of [(Pr 2PCH2)2)Rh((tl cat)-Beat ], HBcat - catecholatoborane, prepared by reaction of [RhQ(N2)(n 3)2] with catecholatoborane, has been reported. The crystal structure of [Rh(dppf)(ii -C5H5)BI%3], ri pf s diphenylphosphinofenocene, has also been described. ... [Pg.342]

Scheme 7.13 Arylation of aldehydes with potassium phenyitrifluoroborate, cataiyzed by Rh-dppf, as described by Batey and coworkers [24]. Scheme 7.13 Arylation of aldehydes with potassium phenyitrifluoroborate, cataiyzed by Rh-dppf, as described by Batey and coworkers [24].

See other pages where Rh-dppf is mentioned: [Pg.143]    [Pg.27]    [Pg.767]    [Pg.28]    [Pg.44]    [Pg.45]    [Pg.45]    [Pg.83]    [Pg.28]    [Pg.44]    [Pg.45]    [Pg.45]    [Pg.83]    [Pg.550]    [Pg.262]    [Pg.315]    [Pg.344]    [Pg.192]    [Pg.194]    [Pg.197]    [Pg.201]    [Pg.158]   
See also in sourсe #XX -- [ Pg.162 ]




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