化学
氧代碳
立体中心
烷基化
催化作用
有机化学
对映选择合成
吲哚试验
氢
试剂
组合化学
化学计量学
手性(物理)
筑地反应
立体选择性
有机催化
化学合成
立体化学
羟醛反应
作者
Guorong Hong,Ran Tao,Liang Wei Benjamin Yep,Bin‐Miao Yang,Gang Liao,Y. Zhao
摘要
The asymmetric synthesis of chiral carbonyl compounds bearing remote stereocenters remains an attractive, yet challenging, goal in modern chemical synthesis. Herein, we report an enantioconvergent approach to γ- and δ-chiral ketones from simple racemic diols through a formal indole alkylation mediated by borrowing hydrogen catalysis. Mechanistic investigations revealed the involvement of a transient oxocarbenium intermediate that plays a key role in the transformation. The development of a new class of iridacycle catalysts featuring a chiral pyrroline backbone proved to be essential for achieving high levels of enantioselectivity. This cascade catalysis process proceeds without stoichiometric reagents and enables the efficient synthesis of a broad range of γ- and δ-chiral ketones in high yields and enantiopurity.
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