Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore, Singapore.
Nat Commun. 2020 Oct 15;11(1):5193. doi: 10.1038/s41467-020-19039-7.
Polyborylated organic compounds have been emerging as versatile building blocks in chemical synthesis. Here we report a selective cobalt-catalyzed deoxygenative 1,1,3-triborylation reaction of allylic ethers with pinacolborane to prepare 1,1,3-triborylalkane compounds. With naturally abundant and/or synthetic cinnamic methyl ethers as starting materials, we have achieved the synthesis of a variety of 1,1,3-triborylalkanes (25 examples). The synthetic utility of these 1,1,3-triborylalkanes is demonstrated through site-selective allylation, protodeborylation, and consecutive carbon-carbon bond-forming reactions. Mechanistic studies including deuterium-labeling and control experiments suggest that this 1,1,3-triborylation reaction proceeds through initial cobalt-catalyzed deoxygenative borylation of allylic ethers to form allylic boronates followed by cobalt-catalyzed 1,1-diborylation of the resulting allylic boronates.
多硼有机化合物已成为化学合成中用途广泛的构建模块。在这里,我们报告了一种钴催化的烯丙基醚与频哪醇硼烷选择性脱氧 1,1,3-三硼化反应,制备 1,1,3-三硼基链烷化合物。以天然丰富的和/或合成肉桂甲基醚作为起始原料,我们已经实现了多种 1,1,3-三硼基链烷(25 个实例)的合成。这些 1,1,3-三硼基链烷的合成用途通过选择性烯丙基化、原脱硼和连续碳-碳键形成反应得到了证明。包括氘标记和对照实验在内的机理研究表明,该 1,1,3-三硼化反应是通过烯丙基醚的钴催化脱氧硼化反应生成烯丙基硼酸酯,然后通过钴催化的生成的烯丙基硼酸酯的 1,1-二硼化反应来进行的。