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

Ramesha, A. R. ; Chandrasekaran, Srinivasan (1994) A facile entry to macrocyclic disulfides: an efficient synthesis of redox-switched crown ethers Journal of Organic Chemistry, 59 (6). pp. 1354-1357. ISSN 0022-3263

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Official URL: http://pubs.acs.org/doi/abs/10.1021/jo00085a025

Related URL: http://dx.doi.org/10.1021/jo00085a025

Abstract

An interesting sulfur transfer reaction with benzyltriethylammonium tetrathiomolybdate has been used efficiently for the synthesis of macrocyclic disufides. 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:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:7148
Deposited On:25 Oct 2010 12:28
Last Modified:03 Feb 2011 06:28

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