TY - JOUR
T1 - Asymmetric homogeneous hydrogenations at scale
AU - Ager, David J.
AU - de Vries, Andre H. M.
AU - de Vries, Johannes G.
PY - 2012
Y1 - 2012
N2 - Asymmetric hydrogenations are increasingly being used to introduce stereogenic centres into products used in the life sciences industries. There are a number of potential pitfalls when moving from a laboratory reaction to a manufacturing process, not least of which is safety. Time-to-market pressure leads to short development times, which in the past could be a large barrier for the implementation of catalytic steps; now there are new ways to minimise this problem. The potential problems associated with impurities and other methods that can shut down the hydrogenation reactions are highlighted in this critical review (353 references).
AB - Asymmetric hydrogenations are increasingly being used to introduce stereogenic centres into products used in the life sciences industries. There are a number of potential pitfalls when moving from a laboratory reaction to a manufacturing process, not least of which is safety. Time-to-market pressure leads to short development times, which in the past could be a large barrier for the implementation of catalytic steps; now there are new ways to minimise this problem. The potential problems associated with impurities and other methods that can shut down the hydrogenation reactions are highlighted in this critical review (353 references).
KW - HIGHLY ENANTIOSELECTIVE HYDROGENATION
KW - BETA-AMINO-ACID
KW - MONODENTATE P-LIGANDS
KW - RHODIUM-CATALYZED HYDROGENATION
KW - FINE CHEMICALS PRODUCTION
KW - BINOL-DERIVED PHOSPHORAMIDITES
KW - UNSATURATED CARBOXYLIC-ACIDS
KW - CHIRAL BISPHOSPHINE LIGAND
KW - DYNAMIC KINETIC RESOLUTION
KW - RESEARCH-AND-DEVELOPMENT
U2 - 10.1039/c2cs15312b
DO - 10.1039/c2cs15312b
M3 - Review article
SN - 0306-0012
VL - 41
SP - 3340
EP - 3380
JO - Chemical Society Reviews
JF - Chemical Society Reviews
IS - 8
ER -