This step involves the introduction of chiral centers in the molecule. For meso-2,6-diaminopimelic acid, this typically means introducing two chiral centers at the 2nd and 6th positions. This can be achieved through reactions with chiral reagents or catalysts.
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3-Oxazolidinecarboxylic acid, 4-(3-hydroxypropyl)-5-oxo-, phenylmethyl ester, (4S)-
ethyl 2,3-di-O-benzyl-5-deoxy-5-C-(4-methoxyphenyl)-β-L-arabinofuranoside
2-Buten-1-one, 1-[(1S,6S)-2,2,6-trimethylcyclohexyl]-, (2E)-
(1S,RS)-3,4-dihydro-6,7-dimethoxy-1-<(p-tolylsulfinyl)-methyl>isoquinoline
ethyl (2R,3S)-2-tert-butoxycarbonylamino-3-(4-(2-methoxyethoxymethoxy)phenyl)-3-methoxypropanoate
(1S,2S,5R)-2-isopropyl-5-methylcyclohexyl 2,4-dinitrophenyl sulfide
4(R)-(tert-butyldimethylsiloxy)-6(R)-<2-<8(S)-(benzyloxy)-1,2,6,7,8,8a(S)-hexahydro-2(S),6(R)-dimethyl-1(S)-naphthyl>ethyl>-2-<(tetrahydropyran-2-yl)oxy>-3,4,5,6-tetrahydro-2H-pyran
(4S,5S)-2-(chloromethyl)-4,5-dihydro-4,5-diphenyl-1-tosyl-1H-imidazole
styrene
Ethyl diazoacetate
(2R,3aR,6aR)-2-Methoxy-hexahydro-cyclopenta[b]furan-4-one
14(R),15(R)-epoxyeicosatrienoic acid
Triethylamine
Phentydrone
