ENANTIOSELECTIVE HYDROGENATION OF ETHYL PYRUVATE IN FLOW REACTOR OVERPt-CD/Si0(2) CATALYSTS
نویسندگان
چکیده
منابع مشابه
Enantioselective hydrogenation of isoquinolines.
Asymmetric hydrogenation of (hetero)arenes is one of the most straightforward ways to synthesize enantiomerically pure, saturated or partially saturated cyclic molecules. Recent progress has significantly expanded the substrate scope of this reaction. Whereas a number of highly efficient catalytic systems have been found for the asymmetric hydrogenation of quinolines, structurally related isoqu...
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Continuous flow systems for hydrogenation using polysilane-supported palladium/alumina (Pd/(PSi-Al(2)O(3))) hybrid catalysts were developed. Our original Pd/(PSi-Al(2)O(3)) catalysts were used successfully in these systems and the hydrogenation of unsaturated C-C bonds and a nitro group, deprotection of a carbobenzyloxy (Cbz) group, and a dehalogenation reaction proceeded smoothly. The catalyst...
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Iridium complexes with chiral N,P ligands have established themselves as efficient catalysts for the asymmetric hydrogenation of olefins, with largely complementary scope to Rh and Ru diphosphane complexes. In contrast to Rh and Ru catalysts, they do not require a coordinating polar group next to the C=C bond. Initial experiments with cationic phosphanyloxazoline (phox) complexes ([Ir(1)(cod)]X...
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Enantioselective hydrogenation of quinoline derivatives catalyzed by phosphine-free chiral cationic Cp*Ir(OTf)(CF 3TsDPEN) complex (CF 3TsDPEN = N-(p-trifluoromethylbenzenesulfonyl)-1,2-diphenylethylene-diamine) afforded the 1,2,3,4-tetrahydroquinoline derivatives in up to 99% ee. The reaction could be carried out with a substrate-to-catalyst molar ratio as high as 1000 in undegassed methanol a...
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ژورنال
عنوان ژورنال: Journal of the Chilean Chemical Society
سال: 2008
ISSN: 0717-9707
DOI: 10.4067/s0717-97072008000400024