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[摘要]:Asymmetric direct aldol reaction of trifluoromethylacetaldehyde with aldehyde using diarylprolinol as a catalyst, to afford a synthetically useful beta-trifluoromethyl-beta-hydroxy aldehyde with excellent enantioselectivity, was developed. Commercially available trifluoromethylacetaldehyde ethyl hemiacetal was used directly as a precursor of trifluoromethylacetaldehyde without acid pyrolysis or distillation prior to use. |
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