The direct catalytic reductive amination of amides remains a challenging transformation, particularly when using weakly nucleophilic amines. However, this strategy offers several synthetic advantages, particularly due to the wide availability of amides, as well as N-sulfonyl and N-sulfinyl amines. We present a mild catalytic approach for the monoalkylation of sulfonamides, sulfamates, sulfamides, and sulfinamides using amides. This protocol exploits the oxophilic character of zirconium, an early, earth-abundant metal, to drive dual reductive cycles and enable the critical amination step. This chemistry is carried out at room temperature using just 10 mol % of Cp2ZrCl2 in combination with hydrosilane reductant, yielding products in up to 94% isolated yield with excellent selectivity. This chemistry enables site-selective monoalkylation of sulfonamides, including examples of late-stage N-alkylation in pharmaceutical applications.

Though precedent remains limited, the selective interhalogenation of allenes offers a valuable synthetic strategy to access products where each halide exhibits orthogonal reactivity. Here, we describe...