“…Most of these studies focused on commercially available 5.0 wt.% Pt/Al 2 O 3 catalysts [7][8][9][10][11][12][13][14][15][16], e.g. E 4759 from Engelhard or JMC 5 R 94 from Johnson Matthey, or 6.3 wt.% Pt/SiO 2 catalysts [17,18], e.g.…”
Platinum nanoparticles supported on periodic mesoporous resols by simple impregnation serve as effective, robust and remarkably reusable catalysts after chirally modified with cinchonidine for the asymmetric hydrogenation of ethyl pyruvate, affording up to 62% enantiomeric excess (ee) and a constant activity after 25th re-use. They can also catalyze the reaction in an environmentally benign manner by using water as a solvent.
“…Most of these studies focused on commercially available 5.0 wt.% Pt/Al 2 O 3 catalysts [7][8][9][10][11][12][13][14][15][16], e.g. E 4759 from Engelhard or JMC 5 R 94 from Johnson Matthey, or 6.3 wt.% Pt/SiO 2 catalysts [17,18], e.g.…”
Platinum nanoparticles supported on periodic mesoporous resols by simple impregnation serve as effective, robust and remarkably reusable catalysts after chirally modified with cinchonidine for the asymmetric hydrogenation of ethyl pyruvate, affording up to 62% enantiomeric excess (ee) and a constant activity after 25th re-use. They can also catalyze the reaction in an environmentally benign manner by using water as a solvent.
“…[110] Kulkarni and Török recently reviewed the application of US activation in heterogeneous catalytic hydrogenations. [28] In many cases, sonochemical activation also resulted in selectivity enhancement; such as in the hydrogenation of α-ketoesters on cinchona alkaloid modified Pt/Al2O3 catalyst, [115] 3-buten-1-ol Sonication resulted in a two-fold increase (~80% overall selectivity compared with 40 %) in CMO formation.…”
REVIEWS
2The reduction of organic compounds via catalytic hydrogenation is an important transformation in organic chemistry, especially in the synthesis of fine chemicals, natural products and pharmaceuticals.
“…According to these initial results, similarly as pointed out by Murakami and coworkers [33], the preparation of the hydroquinoline derivatives was possible over supported Pt catalyst, moreover chiral modification by cinchona alkaloids increased the selectivity of the desired product 5. Although, low ee was obtained in this preliminary study the ee value exceeded the one reported in the hydrogenation of activated benzyl ketones over Pt modified by CD [109]. Thus, based on both the selectivity and the ee obtained, we thought worth studying the effect of the reaction conditions for finding possibilities of increasing these values in this novel asymmetric cascade reaction.…”
Section: Hydrogenation Of 2-nitrophenylpyruvates In Batch Reactormentioning
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