Department of Chemistry, University of Cambridge, United Kingdom.
J Am Chem Soc. 2011 Sep 7;133(35):13778-81. doi: 10.1021/ja206047h. Epub 2011 Aug 17.
A new strategy for the catalytic enantioselective α-arylation of N-acyloxazolidinones with chiral copper(II)-bisoxazoline complexes and diaryliodonium salts is described. The mild catalytic conditions are operationally simple, produce valuable synthetic building blocks in excellent yields and enantioselectivities, and can be applied to the synthesis of important nonsteroidal anti-inflammatory agents and their analogues.
一种新的策略,用于在手性铜(II)-双恶唑啉配合物和二芳基碘鎓盐存在下催化对映选择性 N-酰基恶唑烷酮的α-芳基化反应。温和的催化条件操作简单,以优异的收率和对映选择性得到有价值的合成砌块,可用于合成重要的非甾体抗炎药及其类似物。