189450-22-4Relevant articles and documents
Catalytic hydrogenation of methyl esters of some 1H-pyrazoline-3-carboxylic acids
Gorpinchenko,Petrov,Lozhkin,Galkin,Dokichev
experimental part, p. 1202 - 1207 (2010/04/26)
Hydrogenation over Raney nickel of the methyl ester of 1H-pyrazoline-3- carboxylic acid and also of its 4-phenyl and 5-methoxycarbonyl-substituted analogs, leads respectively to 3-aminopyrrolidin-2-one, its 4-phenyl- and 5-methoxycarbonyl derivatives, pre
Asymmetric synthesis of meso- and (2R,4R)-2,4-diaminoglutaric acids
Avenoza, Alberto,Cativiela, Carlos,Peregrina, Jesus M.,Zurbano, Maria M.
, p. 863 - 871 (2007/10/03)
In order to synthesize meso- and (2R,4R)-2,4-diaminoglutaric acids, a synthetic route has been developed starting from Garner's aldehyde and where the key steps are the asymmetric hydrogenations of (E)- and (Z)-(R)-3-tert-butoxycarbonyl-2,2-dimethyl-4-[2'-(benzamido)-2' -(methoxycarbonyl)ethenyl]-1,3-oxazolidine, under heterogeneous conditions, followed by oxidation and further hydrolysis. A model is proposed to explain the stereochemical outcome of the asymmetric hydrogenation.