The acrolein acetal is then subjected to asymmetric dihydroxylation, a reaction that introduces two hydroxyl groups onto the carbon-carbon double bond of the acrolein moiety. Asymmetric dihydroxylation is often carried out using chiral ligands and oxidizing agents such as OsO? (osmium tetroxide) or other osmium-based catalysts.
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Propanal, 2,3-bis(acetyloxy)-, 1-[(2,4-dinitrophenyl)hydrazone], (S)-
1-Cyclopentene-1-acetic acid, methyl ester
(2R,6R)-2-Hydroxymethyl-6-methyl-piperidine-1-carboxylic acid benzyl ester
1,2-Cyclohexanediol, 1-(4-methoxyphenyl)-, (1R,2R)-rel-
N-[(S)-1-((2R,4S,5S)-5-Methyl-2-phenyl-[1,3]dioxolan-4-yl)-3-oxo-propyl]-acetamide
1-Phenyl-hex-1-yne-3,4-diol
