Posevins Daniels, Bermejo-López Aitor, Bäckvall Jan-E
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, 10691, Stockholm, Sweden.
Department of Natural Sciences, Mid Sweden University, 85170, Sundsvall, Sweden.
Angew Chem Int Ed Engl. 2021 Oct 4;60(41):22178-22183. doi: 10.1002/anie.202106742. Epub 2021 Sep 2.
Herein we disclose an iron-catalyzed cross-coupling reaction of propargyl ethers with Grignard reagents. The reaction was demonstrated to be stereospecific and allows for a facile preparation of optically active allenes via efficient chirality transfer. Various tri- and tetrasubstituted fluoroalkyl allenes can be obtained in good to excellent yields. In addition, an iron-catalyzed cross-coupling of Grignard reagents with α-alkynyl oxetanes and tetrahydrofurans is disclosed herein, which constitutes a straightforward approach towards fully substituted β- or γ-allenols, respectively.
在此,我们公开了一种铁催化的炔丙基醚与格氏试剂的交叉偶联反应。该反应被证明具有立体专一性,并且能够通过有效的手性转移轻松制备光学活性的丙二烯。各种三取代和四取代的氟烷基丙二烯可以以良好至优异的产率获得。此外,本文还公开了一种铁催化的格氏试剂与α-炔基氧杂环丁烷和四氢呋喃的交叉偶联反应,该反应分别构成了一种直接合成全取代β-或γ-烯丙醇的方法。