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Regio- and enantioselective synthesis of allylic fluorides by electrophilic fluorodesilylation of allyl silanes.

机译:通过烯丙基硅烷的亲电氟代脱硅烷基化反应实现烯丙基氟化物的区域和对映选择性合成。

摘要

Enantiopure N-fluorocinchona alkaloids promoted the electrophilic fluorodesilylation of allyl silanes in a conceptually new approach to the regio- and enantioselective formation of allylic fluorides (see scheme). Excellent conversions were observed in these reactions, which afforded the desired allylic fluorides with up to 96% ee.
机译:Enantiopure N-氟金鸡纳生物碱以烯丙基氟化物的区域和对映选择性形成的概念性新方法,促进了烯丙基硅烷的亲电氟去甲硅烷基化反应(参见方案)。在这些反应中观察到优异的转化率,得到具有高达96%ee的所需的烯丙基氟化物。

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