A facile entry to macrocyclic disulfides: an efficient synthesis of redox-switched crown ethers
Data(s) |
25/03/1994
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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 |