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dc.contributor.author
Abonia, Rodrigo  
dc.contributor.author
Castillo, Juan  
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Insuasty, Braulio  
dc.contributor.author
Quiroga, Jairo  
dc.contributor.author
Sortino, Maximiliano Andrés  
dc.contributor.author
Nogueras, Manuel  
dc.contributor.author
Cobo, Justo  
dc.date.available
2018-06-26T23:20:37Z  
dc.date.issued
2016-05  
dc.identifier.citation
Abonia, Rodrigo; Castillo, Juan; Insuasty, Braulio; Quiroga, Jairo; Sortino, Maximiliano Andrés; et al.; Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones; Elsevier; Arabian Journal of Chemistry; 5-2016  
dc.identifier.issn
1878-5352  
dc.identifier.uri
http://hdl.handle.net/11336/50218  
dc.description.abstract
Herein it is provided an efficient, environmentally friendly and one-pot procedure for the synthesis of a library of new and diversely substituted 1,3-thiazolidin-4-ones in short reaction times and good yields through a solvent-, catalyst- and desiccant-free three-component process. Reactions proceeded by treatment of primary benzyl(aryl)amines with aromatic aldehydes (and ketones) and 2-mercaptoacetic acid acting as both reagent and self-catalyst. All reactions were performed in sand bath instead of the commonly used oil bath avoiding the generation of undesired volatile materials proceeding of the thermal decomposition of the oils. IR, Mass and NMR experiments as well as X-ray diffraction confirmed structures of the obtained products.  
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
2-Mercaptoacetic Acid  
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Green Synthesis  
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Multicomponent Reactions  
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Primary Benzylamines  
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Solvent-Free Conditions  
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Thiazolidin-4-Ones  
dc.subject.classification
Otras Ciencias Químicas  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-06-26T22:34:32Z  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Abonia, Rodrigo. Universidad del Valle; Colombia  
dc.description.fil
Fil: Castillo, Juan. Universidad de los Andes; Colombia. Universidad del Valle; Colombia  
dc.description.fil
Fil: Insuasty, Braulio. Universidad del Valle; Colombia  
dc.description.fil
Fil: Quiroga, Jairo. Universidad del Valle; Colombia  
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Fil: Sortino, Maximiliano Andrés. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Química Orgánica. Área Farmacognosia; Argentina  
dc.description.fil
Fil: Nogueras, Manuel. Universidad de Jaén; España  
dc.description.fil
Fil: Cobo, Justo. Universidad de Jaén; España  
dc.journal.title
Arabian Journal of Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.arabjc.2016.11.016  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1878535216302258