Issue 24, 1996

Temperature dependent reversal of enantiomer selectivity in the complexation of optically active phenolic crown ethers with chiral amines

Abstract

Phenolic crown ethers (S,S)-1, (R,R)-2, (S,S)-3 and (S,S)-4 were prepared in enantiomerically pure forms; the enantiomer selectivities of crown ethers (S,S)-1 and (R,R)-2 in complexation with 2-aminopropan-1-ol reversed at ca. 6 °C and increased with increasing temperature above the isoenantioselective temperature.

Article information

Article type
Paper

Chem. Commun., 1996, 2749-2750

Temperature dependent reversal of enantiomer selectivity in the complexation of optically active phenolic crown ethers with chiral amines

K. Naemura, J. Fuji, K. Ogasahara, K. Hirose and Y. Tobe, Chem. Commun., 1996, 2749 DOI: 10.1039/CC9960002749

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements