仙磷
炔丙基
磷化氢
还原消去
化学
催化作用
钯
齿合度
组合化学
配体(生物化学)
药物化学
立体化学
有机化学
生物化学
晶体结构
受体
作者
Huijun Qian,Gabriel N. Morais,Katherine E. Colbaugh,Junqi Su,Zili Chen,Zhiping Li,Shuming Chen,Leiyang Lv
标识
DOI:10.1002/anie.202517878
摘要
Catalyst-controlled divergent transformations represent a vital strategy for the efficient production of structurally diverse molecules from the same readily available precursors. Herein, we report the palladium/phosphine-catalyst-driven chemo- and regiodivergent allyl-propargyl cross-coupling of propargyl carbonates with allyl boronates. Density functional theory (DFT) calculations reveal that the bidentate phosphine ligand plays a crucial role in determining the relative favorability of possible reductive elimination modes from the ƞ3-allyl-ƞ1-allenyl palladium intermediate species. Specifically, MeO-BIPHEP facilitates the 1,1'-reductive elimination to form the 1,4-enallenes; in contrast, XantPhos favors the formation of 1,5-enynes through a 3,3'-reductive elimination pathway.
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