Issue 16, 1984

Synthesis and chiral recognition of optically active crown ethers incorporating a biphenanthryl moiety as the chiral centre

Abstract

Two chiral crown ethers (–)-(S)-(5) and (–)-(R,R)-(6) with a biphenanthryl moiety as the chiral centre have been prepared; examination of their chiral recognition behaviour showed that (–)-(S)-(5) has a very high enantiomer selectivity for 1,2-diphenylethylamine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1111-1112

Synthesis and chiral recognition of optically active crown ethers incorporating a biphenanthryl moiety as the chiral centre

K. Yamamoto, H. Fukushima, Y. Okamoto, K. Hatada and M. Nakazaki, J. Chem. Soc., Chem. Commun., 1984, 1111 DOI: 10.1039/C39840001111

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