首页> 外文期刊>Chemistry: A European journal >Lewis base assisted Br?nsted base catalysis: Direct regioselective asymmetric vinylogous alkylation of allylic sulfones
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Lewis base assisted Br?nsted base catalysis: Direct regioselective asymmetric vinylogous alkylation of allylic sulfones

机译:Lewis碱辅助的Br?nsted碱催化:烯丙基砜的直接区域选择性不对称乙烯基烷基化

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摘要

A Lewis base assisted Br?nsted base catalysis (LBABB) strategy is applied for direct asymmetric vinylogous alkylation of allylic sulfones with Morita-Baylis-Hillman (MBH) carbonates, in which a strong Br?nsted base, tert-butoxy anion, generated in situ from a tertiary amine catalyst and MBH carbonate, is crucial in activating unstabilized nucleophiles. The γ-regioselective alkylation products were obtained with good to excellent enantiomeric excess values when catalyzed by a modified cinchona alkaloid.
机译:刘易斯碱辅助的布朗斯台德碱催化(LBABB)策略被用于与森田-贝利斯-希尔曼(MBH)碳酸酯进行烯丙基砜的直接不对称乙烯基烷基化反应,其中生成了强布朗斯泰德碱,叔丁氧基阴离子。来自叔胺催化剂和MBH碳酸酯的原位反应对于活化不稳定的亲核试剂至关重要。当用修饰的金鸡纳生物碱催化时,获得的γ-区域选择性烷基化产物具有良好的至优异的对映体过量值。

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