Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones

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 pro...

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Autores principales: Abonia, Rodrigo, Castillo, Juan, Insuasty, Braulio, Quiroga, Jairo, Sortino, Maximiliano, Nogueras, Manuel, Cobo, Justo
Formato: article artículo publishedVersion
Lenguaje:Inglés
Publicado: Elsevier 2020
Materias:
Acceso en línea:http://hdl.handle.net/2133/19492
http://hdl.handle.net/2133/19492
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id I15-R121-2133-19492
record_format dspace
institution Universidad Nacional de Rosario
institution_str I-15
repository_str R-121
collection Repositorio Hipermedial de la Universidad Nacional de Rosario (UNR)
language Inglés
orig_language_str_mv eng
topic 2-Mercaptoacetic Acid
Primary Benzylamines
Multicomponent Reactions
Solvent-free Conditions
Green Synthesis
Thiazolidin-4-ones
spellingShingle 2-Mercaptoacetic Acid
Primary Benzylamines
Multicomponent Reactions
Solvent-free Conditions
Green Synthesis
Thiazolidin-4-ones
Abonia, Rodrigo
Castillo, Juan
Insuasty, Braulio
Quiroga, Jairo
Sortino, Maximiliano
Nogueras, Manuel
Cobo, Justo
Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones
topic_facet 2-Mercaptoacetic Acid
Primary Benzylamines
Multicomponent Reactions
Solvent-free Conditions
Green Synthesis
Thiazolidin-4-ones
description 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 Xray diffraction confirmed structures of the obtained products.
format article
artículo
publishedVersion
author Abonia, Rodrigo
Castillo, Juan
Insuasty, Braulio
Quiroga, Jairo
Sortino, Maximiliano
Nogueras, Manuel
Cobo, Justo
author_facet Abonia, Rodrigo
Castillo, Juan
Insuasty, Braulio
Quiroga, Jairo
Sortino, Maximiliano
Nogueras, Manuel
Cobo, Justo
author_sort Abonia, Rodrigo
title Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones
title_short Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones
title_full Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones
title_fullStr Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones
title_full_unstemmed Catalyst-, solvent- and desiccant-free three-component synthesis of novel C-2,N-3 disubstituted thiazolidin-4-ones
title_sort catalyst-, solvent- and desiccant-free three-component synthesis of novel c-2,n-3 disubstituted thiazolidin-4-ones
publisher Elsevier
publishDate 2020
url http://hdl.handle.net/2133/19492
http://hdl.handle.net/2133/19492
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