Nitsch Dominik, Bach Thorsten
Lehrstuhl für Organische Chemie I and Catalysis Research Center (CRC), Technische Universität München , Lichtenbergstr. 4, 85747 Garching, Germany.
J Org Chem. 2014 Jul 3;79(13):6372-9. doi: 10.1021/jo5009993. Epub 2014 Jun 19.
A convergent synthesis of the title compounds is reported, which relies on a successive 2-fold SN'-type substitution reaction at methoxy-substituted propargylic acetates. The furan C3-C4 bond is presumably established by silyl enol ether attack at a propargylic cation intermediate. The resulting α-methoxyallene is intramolecularly substituted, leading to cyclization by displacement of the methoxy group (O-C2 bond formation) and to simultaneous formation of the exocyclic alkene double bond. Despite the relatively mild conditions, the reactions were complete within 5 min.
报道了标题化合物的汇聚合成方法,该方法依赖于在甲氧基取代的炔丙基乙酸酯上连续进行的两次SN'-型取代反应。呋喃的C3-C4键可能是通过硅烯醇醚对炔丙基阳离子中间体的进攻而形成的。生成的α-甲氧基丙二烯发生分子内取代,导致甲氧基被取代(形成O-C2键)并同时形成环外烯烃双键,从而实现环化。尽管反应条件相对温和,但反应在5分钟内即可完成。