Mostrar el registro sencillo del ítem

dc.contributor.author
Fortes, Margiani P.  
dc.contributor.author
Bassaco, Mariana M.  
dc.contributor.author
Kaufman, Teodoro Saul  
dc.contributor.author
Silveira, Claudio C.  
dc.date.available
2016-06-06T21:20:02Z  
dc.date.issued
2014-08  
dc.identifier.citation
Fortes, Margiani P.; Bassaco, Mariana M.; Kaufman, Teodoro Saul; Silveira, Claudio C.; A convenient eco-friendly system for the synthesis of 5-sulfenyl tetrazole; Royal Society of Chemistry; RSC Advances; 4; 65; 8-2014; 34519-34530  
dc.identifier.issn
2046-2069  
dc.identifier.uri
http://hdl.handle.net/11336/6074  
dc.description.abstract
The use of CeCl3·7H2O in polyethyleneglycol 400 (PEG-400), as an efficient and eco-friendly promoter system for the convenient synthesis of 5-sulfenyl tetrazoles derived from indoles and pyrroles, is reported. The synthesis entails the [3 + 2] cycloaddition reaction of NaN3 with 3-thiocyanato indoles (including 3,3′-di-thiocyanato-1H,1H′,2,2′-biindoles) and 2-thiocyanato pyrroles. The thiocyanates were conveniently obtained by the oxone-mediated thiocyanation of differently substituted starting indoles, 1H,1H′,2,2′-biindoles and N-aryl pyrroles with NH4SCN. The scope and limitations of the transformation were also studied.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Royal Society of Chemistry  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc/2.5/ar/  
dc.subject
Eco-.Friendly Synthesis  
dc.subject
5-Sulfenyltetrazoles  
dc.subject
Cerium Catalyst  
dc.subject
Peg-400 as Solvent  
dc.subject.classification
Química Orgánica  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
A convenient eco-friendly system for the synthesis of 5-sulfenyl tetrazole  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-06-01T13:36:14Z  
dc.journal.volume
4  
dc.journal.number
65  
dc.journal.pagination
34519-34530  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Fortes, Margiani P.. Universidade Federal de Santa Maria. Departamento de Química; Brasil  
dc.description.fil
Fil: Bassaco, Mariana M.. Universidade Federal de Santa Maria. Departamento de Química; Brasil  
dc.description.fil
Fil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Instituto de Química Rosario; Argentina  
dc.description.fil
Fil: Silveira, Claudio C.. Universidade Federal de Santa Maria. Departamento de Química; Brasil  
dc.journal.title
RSC Advances  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/content/articlelanding/2014/ra/c4ra05625f  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/C4RA05625F