Department of Chemistry , National University of Singapore , 3 Science Drive 3 , Republic of Singapore 117543.
J Am Chem Soc. 2018 Apr 18;140(15):5257-5263. doi: 10.1021/jacs.8b01561. Epub 2018 Apr 6.
We present herein the first visible-light-driven hydrocarboxylation as well as carbocarboxylation of alkynes using CO via an iridium/cobalt dual catalysis. Such transformations provide access to various pharmaceutically important heterocycles in a one-pot procedure from readily available alkynes. Coumarins, 2-quinolones, and 2-benzoxepinones were directly accessed through a one-pot alkyne hydrocarboxylation/alkene isomerization/cyclization sequence in which the Ir photocatalyst serves a dual role to promote single-electron transfer in alkyne hydrocarboxylation and energy transfer in the subsequent alkene isomerization. Moreover, an unprecedented cobalt carboxylation/acyl migration cascade enables alkyne difunctionalization to introduce γ-hydroxybutenolides with high efficiency. We expect that this cascade strategy will inspire new perspectives for alkyne and alkene difunctionalization.
我们在此展示了首例通过铱/钴双催化作用,利用 CO 在可见光驱动下实现炔烃的氢羧化和碳羧化。此类转化反应可通过炔烃的一锅法氢羧化/烯烃异构化/环化反应序列,从易得的炔烃出发,以一步法得到各种具有重要药用价值的杂环化合物。其中,Ir 光催化剂发挥双重作用,在炔烃氢羧化中促进单电子转移,在随后的烯烃异构化中促进能量转移,从而直接合成香豆素、2-喹诺酮和 2-苯并二氧杂环庚酮。此外,前所未有的钴羧化/酰基迁移级联反应能够高效实现炔烃的双官能团化,引入γ-羟基丁内酯。我们期望这种级联策略将为炔烃和烯烃的双官能团化带来新的视角。