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Nanopalladium catalyst

Scheme 2.17 Heck coupling of aryl chlorides with a nanopalladium catalyst. Scheme 2.17 Heck coupling of aryl chlorides with a nanopalladium catalyst.
Choudary, B.M., Madhi, S., Chowdari, N.S., Kantam, M.L. and Sreedhar, B., Layered double hydroxide supported nanopalladium catalyst for Heck-, Suzuki-, Sonogashira-, and Stille-type coupling reactions of chloroarenes, J. Am. Chem. Soc., 2002, 124, 14127-14136. [Pg.42]

Uozumi Y, Nakao R (2003) Catalytic oxidation of alcohols in water under atmospheric oxygen by use of an amphiphilic resin-dispersion of a nanopalladium catalyst. Angew Chem Int Ed 42(2) 194-197... [Pg.37]

A number of researchers have ttied to tackle catalyst removal/recovery/recycling issues by using systems in which the palladium has been embedded on a solid support. Perhaps the most encouraging example in terms of activation of aryl chlorides is Choudary s heterogeneous layered double hydroxide supported nanopalladium catalyst. This material promotes the coupling of aryl chlorides to phenylacetylene in yields ranging from 60 to 95%. [Pg.5646]

Boronate Microparticle-Supported Nanogold and Nanopalladium Catalysts... [Pg.368]

Yamada YM, Uozumi Y (2006) A solid-phase self-organized catalyst of nanopalladium with main-chain viologen polymers a-alkylation of ketones with primary alcohols. Org Lett 8(7) 1375-1378 Yamada YM, Uozumi Y (2007) Development of a convoluted polymeric nanopalladium catalyst oi-alkylation of ketones and ring-opening alkylation of cyclic 1, 3-diketones with primary alcohols. Tetrahedron 63(35) 8492-8498... [Pg.368]


See other pages where Nanopalladium catalyst is mentioned: [Pg.46]    [Pg.151]    [Pg.382]    [Pg.382]    [Pg.53]    [Pg.297]    [Pg.89]    [Pg.186]    [Pg.27]    [Pg.132]    [Pg.186]    [Pg.155]   
See also in sourсe #XX -- [ Pg.382 ]




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