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Hydrodehalogenation phosphine

Hydrodehalogenation of aliphatic or benzylic halides were catalyzed by water soluble ruthenium phosphine complexes in the presence of sodium formate as hydrogen donor [194], Hydroxycarbonylations could also be performed with high palladium catalyst activities in biphasic systems [195-197]. [Pg.238]

Demchuk, O.M., Yoruk, B., Blackburn, T. and Snieckus, V. (2006) A mixed naphthyl-phenyl phosphine ligand motif for Suzuki, Heck, and hydrodehalogenation reactions. Synlett, 2908-13. [Pg.125]

B nyei., A.C., Lehel, S. and Jo6, F.J., Transfer hydrodehalogenation of organic halides catalyzed by water-soluble ruthenium(II) phosphine complexes, Mol Catal. A Chem., 1997, 116, 349. [Pg.214]

Patzold, E. Ohme, G. (1993) Water-soluble palladium(ll) phosphine complexes as catalysts in the hydrodehalogenation of allyl and benzyl halogenides under biphasic and phase-transfer conditions, J. Prakt. Chem. - Chem. Ztg., 335,181-4. [Pg.217]

See other pages where Hydrodehalogenation phosphine is mentioned: [Pg.207]    [Pg.77]    [Pg.1434]    [Pg.77]    [Pg.288]    [Pg.212]    [Pg.254]    [Pg.254]    [Pg.121]    [Pg.157]    [Pg.245]    [Pg.246]    [Pg.108]    [Pg.900]    [Pg.901]    [Pg.913]    [Pg.913]    [Pg.111]   
See also in sourсe #XX -- [ Pg.346 ]



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