Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance upgrade on Thursday 4th of May 2017 from 8.00am to 9.00am (BST).

During this time our websites will be offline temporarily. If you have any questions please use the feedback button on this page. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 4, 2004
Previous Article Next Article

A novel synthesis of chiral rotaxanes via covalent bond formation

Author affiliations

Abstract

Chiral rotaxanes composed of the asymmetric crownophane incorporating two hydroxy groups as a rotor moiety and the asymmetric axis were effectively synthesized via covalent bond formation, i.e. tandem Claisen rearrangement, esterification, and aminolysis.

Graphical abstract: A novel synthesis of chiral rotaxanes via covalent bond formation

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 14 Nov 2003, accepted on 07 Jan 2004 and first published on 28 Jan 2004


Article type: Communication
DOI: 10.1039/B314744D
Citation: Chem. Commun., 2004, 466-467
  •   Request permissions

    A novel synthesis of chiral rotaxanes via covalent bond formation

    N. Kameta, K. Hiratani and Y. Nagawa, Chem. Commun., 2004, 466
    DOI: 10.1039/B314744D

Search articles by author