Organocatalytic Atroposelective Aldol Condensation: Synthesis of Axially Chiral Biaryls by Arene Formation**

被引:155
作者
Link, Achim [1 ]
Sparr, Christof [1 ]
机构
[1] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
关键词
aldol reaction; atropisomerism; enantioselectivity; organocatalysis; polyketides; NUCLEOPHILIC AROMATIC-SUBSTITUTION; ASYMMETRIC-SYNTHESIS; NATURAL-PRODUCTS; PROLINE; BIOSYNTHESIS; CATALYSIS; OXIDATION; ACID; CD;
D O I
10.1002/anie.201402441
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Axially chiral compounds are of significant importance in modern synthetic chemistry and particularly valuable in drug discovery and development. Nonetheless, current approaches for the preparation of pure atropisomers often prove tedious. We demonstrate here a synthetic method that efficiently transfers the stereochemical information of a secondary amine organocatalyst into the axial chirality of tri-ortho-substituted biaryls. An aromatic ring is formed during the dehydration step of the described aldol condensation cascade, leading to highly enantioenriched binaphthyl derivatives. The fundamental course of the reaction is related to the biosynthesis of aromatic polyketides.
引用
收藏
页码:5458 / 5461
页数:4
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