由Evans恶唑烷酮和/或吡喃糖衍生的光学纯杯[4]芳烃的合成

Bauder Claude, Sémeril David
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引用次数: 0

摘要

描述了八个新的光学纯杯芳烃衍生物,其中它们的下缘被埃文斯恶唑烷酮或吡喃糖取代。所有的大环都通过核磁共振光谱、旋光性和元素分析得到了完整的表征。手性助剂的引入降低了核磁共振观察到的大环的对称性。在埃文斯恶唑烷酮部分上的立体定向烷基化允许在大环的酚位置附近不对称地引入甲基取代基。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of optically pure calix[4]arenes derived from Evans oxazolidinone and/or pyranose
Eight new optically pure calixarene derivatives, in which their lower rims were substituted with Evans oxazolidinone or pyranose moieties, are described. All macrocycles were fully characterized by NMR spectroscopy, optical rotation, and elemental analysis. The introduction of chiral auxiliaries reduced the symmetry of the macrocycle as observed by NMR. Stereospecific alkylation on the Evans oxazolidinone moiety allowed the asymmetric introduction of a methyl substituent near a phenolic position of the macrocycle.
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