Desymmetrization of Phosphinic Acids via Pd-Catalyzed Asymmetric Allylic Alkylation: Rapid Access to P-Chiral Phosphinates

被引:47
|
作者
Trost, Barry M. [1 ]
Spohr, Simon M. [1 ]
Rolka, Alessa B. [1 ]
Kalnmals, Christopher A. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
ENANTIOSELECTIVE SYNTHESIS; STEREOGENIC PHOSPHINAMIDES; OXIDES; LIGANDS; HYDROGENATIONS; ARYLATION; OXIDATION; RHODIUM; ROUTE;
D O I
10.1021/jacs.9b07340
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis of P-chiral compounds is challenging, especially since useful catalytic methods for preparing such molecules are scarce. Herein we disclose a desymmetrization that employs phosphinic acids as prochiral nucleophiles in a Pd-catalyzed asymmetric allylic alkylation reaction, furnishing phosphinates with high enantio- and diastereoselectivity. This new method has broad scope and is applied to the synthesis of an enantioenriched tertiary phosphine oxide.
引用
收藏
页码:14098 / 14103
页数:6
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