Merging Cobalt-Catalyzed C–H Activation with the Mannich Reaction: A Modular Approach to α‑Substituted N‑Sulfonyl Amines
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https://figshare.com/articles/dataset/Merging_Cobalt-Catalyzed_C_H_Activation_with_the_Mannich_Reaction_A_Modular_Approach_to_Substituted_i_N_i_Sulfonyl_Amines/25745174
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A three-component synthesis of α-substituted N-sulfonyl amines from aryl aldehydes, primary sulfonamides, and (hetero)arenes is described. This transformation enables a straightforward and modular synthesis of highly substituted sulfonamide scaffolds in good yields. The direct functionalization of C(sp2)–H bonds via cobalt-catalyzed C–H-activation offers an appealing and atom-economical alternative to classical methods for the synthesis of α-arylated amines such as the Petasis or Mannich-type reactions.



