化学
电化学
杂原子
烷基
亲核细胞
反应性(心理学)
组合化学
表面改性
有机化学
立体化学
电极
物理化学
医学
替代医学
病理
催化作用
作者
Markus D. Schoetz,Kristina Deckers,Gurdeep Singh,Eric Ahrweiler,Annika Hoeppner,Franziska Schoenebeck
摘要
Because of their robustness and orthogonal reactivity features, alkyl germanes bear significant potential as functional handles for the construction of C(sp3)-rich scaffolds, especially in the context of modular synthetic approaches. However, to date, only radical-based reactivity has been accessible from these functional handles, which limits the types of possible decorations. Here, we describe the first general C(sp3)–heteroatom bond formation of alkyl germanes (−GeEt3) by leveraging electrochemistry to unlock polar reactivity. This approach allowed us to couple C(sp3)–GeEt3 with a variety of nucleophiles to construct ethers, esters, amines, amides, sulfonamides, sulfides, as well as C–P, C–F, and C–C bonds. The compatibility of the electrochemical approach with a modular synthetic strategy of a C1 motif was also showcased, involving the sequential functionalization of Cl, Bpin, and ultimately GeEt3 via electrochemistry.
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