对称化
对映选择合成
分子内力
催化作用
产量(工程)
化学
芳基
组合化学
立体化学
药物化学
有机化学
材料科学
冶金
烷基
作者
Weiwei Zi,F. Dean Toste
标识
DOI:10.1002/anie.201508331
摘要
A gold(I)-catalyzed enantioselective desymmetrization of 1,3-diols was achieved by intramolecular hydroalkoxylation of allenes. The catalyst system 3-F-dppe(AuCl)2/(R)-C8-TRIPAg proved to be specifically efficient to promote the desymmetrizing cyclization of 2-aryl-1,3-diols, which have proven challenging substrates in previous reports. Multisubstituted tetrahydrofurans were prepared in good yield with good enantioselectivity and diastereoselectivity by this method.
科研通智能强力驱动
Strongly Powered by AbleSci AI