Electrochemistry-Enabled C-Heteroatom Bond Formation of Alkyl Germanes

Abstract

Because of their robustness and orthogonal reactivity features, alkyl germanes bear significant potential as functional handles for the construction of C(sp 3 )-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(sp 3 )−heteroatom bond formation of alkyl germanes (−GeEt 3 ) by leveraging electrochemistry to unlock polar reactivity. This approach allowed us to couple C(sp 3 )−GeEt 3 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 C 1 motif was also showcased, involving the sequential functionalization of Cl, Bpin, and ultimately GeEt 3 via electrochemistry.