化学
羰基化
钯
催化作用
甲酸
异构化
区域选择性
有机化学
组合化学
一氧化碳
作者
Rui Sang,Peter Kucmierczyk,Kaiwu Dong,Robert Franke,Helfried Neumann,Ralf Jackstell,Matthias Beller
摘要
A general and selective palladium-catalyzed alkoxycarbonylation of all kinds of alkenes with formic acid (HCOOH, FA) is described. Terminal, di-, tri-, and tetra-substituted including functionalized olefins are converted into linear esters with high yields and regioselectivity. Key-to-success is the use of specific palladium catalysts containing ligands with built-in base, e.g., L5. Comparison experiments demonstrate that the active catalyst system not only facilitates isomerization and carbonylation of alkenes but also promotes the selective decomposition of HCOOH to CO under mild conditions.
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