Review reveals strategies for site-selective C-H functionalization using traceless nitrogen-based directing groups, highlighting efficient pathways for drug synthesis.
The chelation‐assisted CH bond activation with proper directing groups not only promotes the reaction efficiency but also enables selective CC or CX bond formation at the specific positions. Among them, the traceless directing groups (TDGs) strategy is highly attractive since it allows the in situ removal of directing groups after the directed CH bond functionalization. On the other hand, N ‐containing substrates, e.g., N ‐heterocycles, amines, and oximes, are of great importance in both organic synthesis and drug discovery. The directed site‐selective CH bond functionalization of nitrogen‐based substrates using TDG strategy constitutes an ideal solution to access more elaborate molecules. In this context, this review focus on the development of diverse traceless N ‐functionalized directing groups and their application in the CH bond functionalization, along with mechanistic insights into the directing group removal steps. Typical examples that use N ‐functionalized TDGs, such as N ‐oxides, nitrones, N ‐nitroso groups, hydrazyl groups, N ‐acyl groups, and other nitrogen‐functionalized groups, have been documented in this review, aiming to give a timely comprehensive overview and stimulate the development of more efficient methodologies.
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Liu et al. (2026) studied this question.
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