Chiral auxiliaries are molecules or groups temporarily attached to a molecule to induce chirality. They are commonly used in asymmetric synthesis to prepare enantiomerically pure compounds from prochiral or meso compounds. This allows the creation of molecules with well-defined stereochemistry.
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(1S,5S)-spiro[1,5-benzodithiepane-3,7'-[3'-(benzyloxycarbonyl)-[3]aza-[6,8]dioxabicyclo[3.3.0]octane]] 1,5-dioxide
2-Phenyl-cyclopropanecarboxylic acid 1-isopropyl-1,2-dimethyl-propyl ester
ethyl 3E-<(1R,2S)-2-phenyl-1-cyclopropyl>prop-1-enoate
(2S,3S,SS)-3-(2,4-dinitrophenyl)-2-(p-tolylsulfinyl)oxirane
Benzaldehyde
(-)-(S)-3-vinylcyclohex-2-en-1-yl benzoate
(1S,3S)-3-Benzenesulfonyl-4-methyl-1-phenyl-pent-4-en-1-ol
ethyl (1R)-2-hydroxy-1-phenylethylcarbamate
1-Bromo-4-tert-butyl-2-nitrobenzene
1,3,6-tri-O-acetyl-4-O-benzyl-2-O-[(R)-α-(ethoxycarbonyl)benzyl]-α-D-glucopyranose
(1S,7R)-4-Thia-tricyclo[5.2.1.02,6]dec-8-ene 4,4-dioxide
(R)-1-phenyl-1-tetradecanol
C23H29NO3
(1S,4R,7R,8S)-7-(4-bromophenyl)-5,5-dimethyl-8-nitrobicyclo[2.2.2]octan-2-one
(R)-tylophorine
(4S,4'S,5S,5'S)-2,2'-(4-vinylpyridine-2,6-diyl)bis(4,5-diphenyl-4,5-dihydrooxazole)
(R(S),4S)-4-phenyl-N-(trifluoromethanesulfinyl)oxazolidin-2-one
