Issue 14, 1983

Synthesis and chiral recognition of novel crown ethers incorporating helicene chiral centres

Abstract

Two novel optically active crown ethers (7) and (14) incorporating helicene molecular frameworks were prepared, and their chiral recognition properties were examined to show that (M)-(–)-(7) and (M)-(–)-(14) had opposite chiral recognition for the transport of methyl phenylglycinate or 1-phenylethylamine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 787-788

Synthesis and chiral recognition of novel crown ethers incorporating helicene chiral centres

M. Nakazaki, K. Yamamoto, T. Ikeda, T. Kitsuki and Y. Okamoto, J. Chem. Soc., Chem. Commun., 1983, 787 DOI: 10.1039/C39830000787

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