Industrial Application of Enantioselective Hydrogenation: Where Do You Get the Chiral Catalyst?

ChemInform ◽  
2003 ◽  
Vol 34 (27) ◽  
Author(s):  
Marc Thommen ◽  
Hans-Ulrich Blaser
2006 ◽  
Vol 88 (2) ◽  
pp. 391-398 ◽  
Author(s):  
György Szöllősi ◽  
Beáta Hermán ◽  
Ferenc Fülöp ◽  
and Mihály Bartók

1996 ◽  
Vol 7 (4) ◽  
pp. 1011-1018 ◽  
Author(s):  
Hans-Jörn Kreuzfeld ◽  
Ute Schmidt ◽  
Christian Döbler ◽  
Hans Walter Krause

2004 ◽  
Vol 59 (4) ◽  
pp. 468-477 ◽  
Author(s):  
Lutz F. Tietze ◽  
Nils Rackelmann

AbstractThe domino Knoevenagel-hetero-Diels-Alder reaction of the aldehyde rac-8, Meldrum’s acid 2 and enol ether 3 leads to the cycloadduct rac-17 as the main product which in a second domino process was transformed into the benzoisoquinolizidine rac-18 by solvolysis, hydrogenolysis, condensation and hydrogenation; rac-18 was used as a substrate for the synthesis of the two diastereomeric epiemetine analogues 9 and 10 with > 96% ee (9) and 80% ee (10), respectively, by condensation with the phenylethylamine 23, Bischler-Napieralski reaction and “enantioselective” hydrogenation using the chiral catalyst (R,R)-26.


1994 ◽  
Vol 368 ◽  
Author(s):  
Kam T. Wan ◽  
Mark E. Davis

ABSTRACTThe application of heterogeneous asymmetric catalysis to fine chemicals synthesis is discussed. The asymmetric synthesis of naproxen, a non-steroidal antiinflammatory drug, using a novel, heterogeneous, chiral catalyst is used as an example to illustrate the feasibility to industrial application.


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