Functionalized olefin cross-coupling to construct carbon-carbon bonds | |
Article | |
关键词: CONJUGATE ADDITION; UNACTIVATED OLEFINS; TERTIARY ALCOHOLS; HYDROGENATION; REAGENTS; ESTERS; PHENYLSILANE; CHEMISTRY; MECHANISM; RADICALS; | |
DOI : 10.1038/nature14006 | |
来源: SCIE |
【 摘 要 】
Carbon-carbon (C-C) bonds form the backbone of many important molecules, including polymers, dyes and pharmaceutical agents. The development of new methods to create these essential connections in a rapid and practical fashion has been the focus of numerous organic chemists. This endeavour relies heavily on the ability to form C-C bonds in the presence of sensitive functional groups and congested structural environments. Here we report a chemical transformation that allows the facile construction of highly substituted and uniquely functionalized C-C bonds. Using a simple iron catalyst, an inexpensive silane and a benign solvent under ambient atmosphere, heteroatom-substituted olefins are easily reacted with electron-deficient olefins to create molecular architectures that were previously difficult or impossible to access. More than 60 examples are presented with a wide array of substrates, demonstrating the chemoselectivity and mildness of this simple reaction.
【 授权许可】
Free