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Palladium on pumice: new catalysts for the stereoselective semihydrogenation of alkynes to (Z)-alkenes

✍ Scribed by Michelangelo Gruttadauria; Leonarda F Liotta; Renato Noto; Giulio Deganello


Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
62 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis


High selectivities (93-99%) and excellent stereoselectivities (>99%) in the semihydrogenation of C C triple bonds were achieved using palladium on pumice with a metal loading of 0.5, 1.5 or 3.0% wt as catalyst. The reactions were carried out in ethanol or tetrahydrofuran with only 2.5% of ethylenediamine allowing a self-terminating semihydrogenation independently on the C C triple bond.


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