Sun Yin-Wei, Tang Xiang-Ying, Shi Min
Key Laboratory for Advanced Materials and Institute of Fine Chemicals, School of Chemistry & Molecular Engineering, East China University of Science and Technology, and 130 MeiLong Road, Shanghai 200237, People's Republic of China.
Chem Commun (Camb). 2015 Sep 21;51(73):13937-40. doi: 10.1039/c5cc05808b.
The synthesis of medium-sized heterocycles possessing a trans double bond is still a challenge. Herein, gold(I)-catalyzed 1,2-acyloxy migration/intramolecular cyclopropanation/ring enlargement cascade reaction of furans has been developed, providing highly efficient access to ten- and eleven-membered heterocycles with a broad substrate scope under mild reaction conditions. The reaction outcome features high chemoselectivity at the C5-position of furan. Moreover, a trans-double bond was embodied in the medium ring system.
合成具有反式双键的中等大小杂环仍然是一项挑战。在此,已开发出金(I)催化的呋喃的1,2-酰氧基迁移/分子内环丙烷化/环扩大级联反应,在温和的反应条件下为具有广泛底物范围的十元及十一元杂环提供了高效的合成方法。该反应结果在呋喃的C5位具有高化学选择性。此外,在中环体系中体现了一个反式双键。