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


Autoria(s): Ramesha, AR; Chandrasekaran, S
Data(s)

25/03/1994

Resumo

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.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/36111/1/a_facile.pdf

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.

Publicador

American Chemical Society

Relação

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

http://eprints.iisc.ernet.in/36111/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed