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A Versatile, Traceless C–H Activation-Based Approach for the Synthesis of Heterocycles

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/A_Versatile_Traceless_C_H_Activation_Based_Approach_for_the_Synthesis_of_Heterocycles/3207523
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A versatile, traceless C–H activation-based approach for the synthesis of diversified heterocycles is reported. Rh­(III)-catalyzed, N-amino-directed C–H alkenylation generates either olefination products or indoles (in situ annulation) in an atom- and step-economic manner at room temperature. The remarkable reactivity endowed by this directing group enables scale-up of the reaction to a 10 g scale at a very low catalyst loading (0.01 mol %/0.1 mol %). Ex situ annulation of olefination product provides entry into an array of heterocycles.
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2016-05-16
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