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有机催化蒽酮与β-硝基烯烃的不对称Michael加成反应 被引量:4

Organocatalytic Asymmetric Michael Addition of Anthrone with β-Nitroolefins
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摘要 将金鸡纳生物碱衍生物用于催化蒽酮和β-硝基芳基乙烯的不对称Michael加成反应。考察了溶剂、温度及催化剂用量对反应催化性能的影响。结果表明,最佳条件为5%(摩尔分数)催化剂1b、甲苯为溶剂、0℃反应,得到了91%~99%的化学产率和最高达95%ee的对映体选择性。 Cinchona alkaloid derivatives as organocatalysts were applied in asymmetric Michael addition reaction of anthrone with various trans-β-nitroolefins. Solvent, temperature and catalyst loading were screened. The optimized conditions are using toluene as the solvent with a 5% (molar fraction) loading of catalyst lb at room temperature. The products are obtained in 91% -99% yield with up to 95% ee.
出处 《应用化学》 CAS CSCD 北大核心 2015年第4期422-427,共6页 Chinese Journal of Applied Chemistry
基金 国家自然科学基金(21102055) 吉林省自然科学基金(201015237)资助项目~~
关键词 金鸡纳生物碱衍生物 有机催化 不对称MICHAEL加成反应 蒽酮 β-硝基烯烃 Cinchona alkaloid derivative organocatalysis asymmetric Michael addition anthrone β-nitroolefins
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参考文献17

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