Bergamaschi Enrico, Lunic Danijela, McLean Liam A, Hohenadel Melissa, Chen Yi-Kai, Teskey Christopher J
Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.
Angew Chem Int Ed Engl. 2022 Feb 14;61(8):e202114482. doi: 10.1002/anie.202114482. Epub 2022 Jan 11.
The ability to selectively react one functional group in the presence of another underpins efficient reaction sequences. Despite many designer catalytic systems being reported for hydroboration reactions, which allow introduction of a functional handle for cross-coupling or act as mild method for reducing polar functionality, these platforms rarely deal with more complex systems where multiple potentially reactive sites exist. Here we demonstrate, for the first time, the ability to use light to distinguish between ketones and carboxylic acids in more complex molecules. By taking advantage of different activation modes, a single catalytic system can be used for hydroboration, with the chemoselectivity dictated only by the presence or absence of visible light.
在另一个官能团存在的情况下选择性地使一个官能团发生反应的能力是高效反应序列的基础。尽管已经报道了许多用于硼氢化反应的设计催化体系,这些体系允许引入用于交叉偶联的官能团手柄或作为还原极性官能团的温和方法,但这些平台很少处理存在多个潜在反应位点的更复杂体系。在这里,我们首次展示了在更复杂的分子中利用光来区分酮和羧酸的能力。通过利用不同的活化模式,单一催化体系可用于硼氢化反应,化学选择性仅由可见光的存在与否决定。