This term refers to a reaction or process that generates a single enantiomer (mirror-image isomer) of a chiral molecule. Enantiospecific reactions are crucial in asymmetric synthesis to obtain optically pure compounds.
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(3S,4R)-1-Isopropyl-4-methyl-3-phenyl-azetidin-2-one
(R,E)-4-phenylbut-3-en-2-yl pivalate
Butanoic acid, 4-oxo-3-[(9-phenyl-9H-fluoren-9-yl)amino]-, methyl ester, (3S)-
(3R,4S,4'S,5'S) N-(p-anisyl)-3-benzyloxy-4-
Benzyl-[1-((4S,5R,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-yl)-meth-(Z)-ylidene]-amine
(3R,4R)-cis-1-(p-anisyl)-3-azido-4-carbomethoxyazetidin-2-one
(+)-[(1S,2R)-2-bromo-1-chloropropyl]benzene
(3R,4R,5R)-4-Benzyloxy-5-pentyl-tetrahydro-furan-2,3-diol
2S,1'R-ethyl-(1'-benzoyloxyethyl)-5-hexenoate
(R)-2,2-Dimethyl-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-oxazolidine-3-carboxylic acid methyl ester
(2R,3S)-2-benzyloxy-3-fluoro-5-hexenal
Benzenemethanol, -alpha--(aminomethyl)-2-methyl-, (R)- (9CI)
(S,E)-2-(2-(benzyloxy)ethyl)-2-ethylpent-3-en-1-ol
(5S)-5-[(1S,2R,3S)-1,2,3-trihydroxy-3-phenylpropyl]furan-2(5H)-one
OCTAHYDRO-INDOLIZINE-6,7-DIOL
(4S,5S)-1-benzyl-5-(2IV-chloroacetyl)-2-oxo-3-(9''-phenylfluoren-9''-yl)imidazolidine-4-carboxylic acid methyl ester
2-epi-valienamine
(2S,3S) benzyl 2-
