Hydrogenation is a chemical reaction in which hydrogen gas (H2) is added to a compound. In asymmetric hydrogenation, the hydrogenation process is carried out in such a way that one enantiomer (mirror image) of the product is favored over the other. This results in the formation of chiral compounds with high enantioselectivity.
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thiophene-2-(N-diphenylphosphino)methylamine
2-(2-Naphthyl)-4,6-diphenylphosphinine
(R)-2-Acetylamino-3-(4-acetyl-3-methoxy-phenyl)-propionic acid
2-isopropyl-3-{2-[3-methoxy(propyloxy)]-4-methoxyphenyl}propionic acid
(R)-(E)-1,3-diphenyl-prop-2-en-1-ol
(S)-(-)-α-(dimethoxy-3,4 benzyl)hemisuccinate de methyle
5-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-2,6-dimethyl-nicotinic acid tert-butyl ester
triphenylphosphine
Pyridine
(S)-(1-(3’-aminophenyl)ethanol)
Phosphine, (5,5'-dimethoxy-4,4',6,6'-tetramethyl[1,1'-biphenyl]-2,2'-diyl)bis[diphenyl- , (R)-
(3R) methyl β-hydroxy-β-(p-methoxyphenyl) propionate
(1R,2S)-2-methoxy-1-phenyl-1-propanol
Bicyclo[2.2.1]heptane-1-carbonyl chloride, 7,7-dimethyl-2-oxo-, (1S,4R)-
(R)-N-(Pyridin-2-ylmethyl)-7′-di( 3,5-di-tert-butylphenyl)phosphin o-1,1′-spirobiindanyl-7-amine
(S)-2-amino-3-phenyl-N-[(R)-1-phenylethyl]propanamide
Indolizine, 7-methyl-2-phenyl-
2-bromophenyl ferrocenyl methanol
BIS(3,5-DIMETHYL-4-METHOXYPHENYL)PHOSPHINE
(3R)-8-hydroxy-7-(3-hydroxy-3-phenylpropyl)-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxylic acid dimethylamide
(S)-3-((6-((2-(tert-butylcarbamoyl)pyrrolidin-1-yl)methyl)-pyridin-2-yl)methyl)-1-(2,6-diisopropylphenyl)-1H-imidazol-3-ium bromide
