After the reaction, the diastereomeric salt or complex is usually not soluble in the reaction solvent and can be precipitated out. This is typically achieved by adding a non-solvent or adjusting the pH of the reaction mixture.
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(R)-3-amino-3-phenylprop-1-yne
phthalimide
triphenylphosphine
methyl 2-(phenylmethylsulfanyl)-3,5-dinitrobenzenecarboxylate
N-(2,4-dinitrobenzylidene)-2,4-dimethoxyaniline
5-Pyrimidinecarbonitrile, 1,2,3,4-tetrahydro-2,4-dioxo-6-phenyl-
(S)-6-[{3-[3-dimethylaminopropyl(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-2-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyllamino]hexanoic acid tert-butyl ester
3,3'-(1,3-butadiyne-1,4-diyl)bis<2-(phenylmethoxy)pyridine>
H-GLY-D-GLN-OH
N4-(4-methylphenyl)-3,4-Pyridinediamine
5-[ISOCYANO-(TOLUENE-4-SULFONYL)-METHYL]-BENZO[1,3]DIOXOLE
