Highly enantioselective Michael-aldol-dehydration reaction for the synthesis of chiral 3,5-diaryl-cyclohexenones catalyzed by primary amine
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文摘
A simple organocatalytic Michael-aldol-dehydration domino approach to chiral 3,5-diaryl-cyclohexenones from acetone and α,β-unsaturated ketones was developed for the first time using a simple chiral primary amine as a catalyst. Moderate to good yields (up to 85%) and excellent enantioselectivities (88–98% ee) were obtained.

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