A facile entry to macrocyclic disulfides: an efficient synthesis of redox-switched crown ethers

Ramesha, AR and Chandrasekaran, S (1994) A facile entry to macrocyclic disulfides: an efficient synthesis of redox-switched crown ethers. In: Journal of Organic Chemistry, 59 (6). 1354 -1357.

PDF a_facile.pdf - Published Version Restricted to Registered users only Download (397kB) | Request a copy

Abstract

An interesting sulfur transfer reaction with benzyltriethylammonium tetrathiomolybdate has been used efficiently for the synthesis of macrocyclic disulfides. This methodology has been extended to a high-yield synthesis of ''redox-switched'' crown ethers which have potential application for selective ion transport across liquid membranes.

Item Type:	Journal Article
Publication:	Journal of Organic Chemistry
Publisher:	American Chemical Society
Additional Information:	Copyright of this article belongs to American Chemical Society.
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	03 Jun 2011 07:22
Last Modified:	03 Jun 2011 07:22
URI:	http://eprints.iisc.ac.in/id/eprint/36111

Actions (login required)

View Item