阿托品
酰胺
化学
立体选择性
对映选择合成
羟醛缩合
冷凝
胺气处理
反应性(心理学)
有机化学
戒指(化学)
组合化学
羟醛反应
催化作用
热力学
病理
替代医学
医学
物理
作者
Vincent C. Fäseke,Christof Sparr
标识
DOI:10.1002/anie.201602689
摘要
The increasing awareness of the importance of amide atropisomers prompts the development of novel strategies for their selective preparation. Described herein is a method for the enantioselective synthesis of atropisomeric aromatic amides by an amine-catalyzed arene-forming aldol condensation. The high reactivity of the glyoxylic amide substrates enables a remarkably efficient construction of a new aromatic ring, which proceeds within minutes at ambient temperature to afford products with excellent stereoselectivity. The high rotational barriers of the reduced products highlight the utility of this stable, spatially organized chiral scaffold.
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