Ren Hai, Wang Pan, Wang Lijia, Tang Yong
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , 345 Lingling Lu, Shanghai 200032, P. R. China.
Org Lett. 2015 Oct 2;17(19):4886-9. doi: 10.1021/acs.orglett.5b02440.
A highly enantioselective and regioselective chiral Lewis acid catalyzed tandem Friedel-Crafts/lactonization reaction is reported, providing direct access to plenty of 3-hydroxy-3-trifluoromethyl benzofuran-2-ones in up to 94% yields with up to >99% ee. Mechanistic study reveals that the interactions between the phenolic hydroxyl group and trifluoropyruvate are the most likely contributing factor to the high enantio- and regioselectivity. Optically pure (-)-BHFF can be obtained in gram-scale with 0.05 mol % catalyst, demonstrating the potentially utility of this method in medicinal chemistry.
报道了一种高度对映选择性和区域选择性的手性路易斯酸催化的串联傅克/内酯化反应,可直接获得大量的3-羟基-3-三氟甲基苯并呋喃-2-酮,产率高达94%,对映体过量率高达>99%。机理研究表明,酚羟基与三氟丙酮酸之间的相互作用最有可能是高对映选择性和区域选择性的原因。使用0.05 mol%的催化剂可克级规模获得光学纯的(-)-BHFF,证明了该方法在药物化学中的潜在应用价值。