Mostrar el registro sencillo del ítem

dc.contributor.author
Kuhn, Bruna L.  
dc.contributor.author
Fortes, Margiani P.  
dc.contributor.author
Kaufman, Teodoro Saul  
dc.contributor.author
Silveira, Claudio C.  
dc.date.available
2016-06-02T18:39:09Z  
dc.date.issued
2014-02  
dc.identifier.citation
Kuhn, Bruna L.; Fortes, Margiani P.; Kaufman, Teodoro Saul; Silveira, Claudio C.; Facile, efficient and eco-friendly synthesis of 5-sulfenyl tetrazole derivatives of indoles and pyrroles; Elsevier; Tetrahedron Letters; 55; 9; 2-2014; 1648-1652  
dc.identifier.issn
0040-4039  
dc.identifier.uri
http://hdl.handle.net/11336/6013  
dc.description.abstract
A concise, two-step eco-friendly approach towards the synthesis of 5-sulfenyl tetrazole derivatives of indoles and pyrroles, is reported. The synthesis comprises the oxone-mediated thiocyanation of the starting heterocycles towards intermediate 3-thiocyanato indoles and 2-thiocyanato pyrroles, and their subsequent treatment with sodium azide in 2-propanol/water under zinc bromide promotion.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
5-Sulfenyl Tetrazoles  
dc.subject
Pyrrole And Indole Derivatives-Thiocyanation  
dc.subject
Eco-Friendly Functionalization of Heterocycles  
dc.subject
Zinc Bromide Promoted Reaction  
dc.subject.classification
Química Orgánica  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Facile, efficient and eco-friendly synthesis of 5-sulfenyl tetrazole derivatives of indoles and pyrroles  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-06-01T13:36:10Z  
dc.journal.volume
55  
dc.journal.number
9  
dc.journal.pagination
1648-1652  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Kuhn, Bruna L.. Universidade Federal de Santa Maria. Departamento de Química; Brasil  
dc.description.fil
Fil: Fortes, Margiani P.. 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
Tetrahedron Letters  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403914001476  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2014.01.101  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.tetlet.2014.01.101  

Archivos asociados
Thumbnail
 
Tamaño: 616.0Kb
Formato: PDF
.