Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gujarat 380054, India.
Org Biomol Chem. 2020 Nov 7;18(41):8346-8365. doi: 10.1039/d0ob01382j. Epub 2020 Oct 6.
Potassium tertiary butoxide (KOBu) mediated constructions of C-C, C-O, C-N, and C-S bonds are reviewed with special emphasis on their synthetic applications. KOBu can be used to perform reactions already known to be carried out using transition metals, but it has advantages in terms of environmental congruence and economic cost. KOBu is widely employed in organic synthesis to mediate the construction of C-C, C-O, C-N, C-S and miscellaneous bonds in good to excellent yields. Synthetic uses of KOBu in coupling, alkylation, arylation, α-phenylation, cyclization, Heck-type, annulation, photo-arylation, aromatic-substitution, amidation, and silylation reactions are summarized and discussed. The mechanisms through which KOBu carries out a specific reaction are also discussed. One of the goals of this review is to attract the attention of chemists as to the benefits of using KOBu as an environmentally benign alternative to transition metals and its applications in the construction of chemical bonds with predominant importance in organic synthesis. This review completely covers the synthetic protocols that have been performed using KOBu in the last two decades.
叔丁醇钾(KOBu)介导的 C-C、C-O、C-N 和 C-S 键的构建反应综述,特别强调了它们在合成中的应用。KOBu 可用于进行已经使用过渡金属进行的反应,但在环境一致性和经济成本方面具有优势。KOBu 在有机合成中广泛用于介导 C-C、C-O、C-N、C-S 和杂键的构建,收率良好至优秀。KOBu 在偶联、烷基化、芳基化、α-芳基化、环化、Heck 型、环化、光芳基化、芳香取代、酰胺化和硅烷基化反应中的合成用途进行了总结和讨论。还讨论了 KOBu 进行特定反应的机制。本文综述的目的之一是引起化学家的注意,即使用 KOBu 作为环境友好的过渡金属替代物的好处,以及其在构建在有机合成中具有重要意义的化学键中的应用。本综述完全涵盖了过去二十年中使用 KOBu 进行的合成方案。