The nucleophilic attack by the amine introduces chirality into the molecule. The resulting product will be a chiral compound, as opposed to the symmetrical starting material (meso-epoxide).
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C12H16FNO
2C-D
(3R,4R)-3,4-Bis-benzyloxy-1-((E)-but-2-enyl)-pyrrolidine-2,5-dione
(R)-(-)-p-(2-methylhexyl)nitrobenzene
4
(6R)-2-<(R)-2-hydroxy-2-phenylacetyl>-6-<(S)-5-methoxycarbonyl-2-oxo-pyrrolidine-1-yl>-3,6-dihydro-2H-1,2-oxazine
(3R,3aR,7aR)-hexahydro-3-(p-methoxyphenylamino)-2(3H)-benzofuranone
Ethyl acetate
(2R,3R)-methyl 4-nitro-2-phenyl-3-(4-(trifluoromethyl)phenyl)-2,3-dihydro-1H-pyrrole-2-carboxylate
1-Bromo-5-phenyl-spiro[2.5]oct-4-ene
(2S,3S)-2-Isopropyl-3-(4-methoxy-benzylamino)-5-trimethylsilanyl-pent-4-ynethioic acid S-tert-butyl ester
(E)-N-(4,4-dimethylpent-2-enyl)benzenamine
5-tert-butyl-2-chloro-1-cyclohexene-1-methanol
C19H25NO5S
(2S,3S)-2-methylpentane-1,3-diol
2-Imidazolidinone, 1,3-dimethyl-4,5-diphenyl-, (4S,5S)-
(S)-2-N,N-dibenzylamino-3-cyanopropanoic acid benzyl ester
2,3-butadienyl-2-methylallyl-bis(phenylsulfonyl)methane
