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: | , , , , , , |
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Formato: | article artículo publishedVersion |
Lenguaje: | Inglés |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | http://hdl.handle.net/2133/19492 http://hdl.handle.net/2133/19492 |
Aporte de: |
id |
I15-R121-2133-19492 |
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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 |
work_keys_str_mv |
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bdutipo_str |
Repositorios |
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1764820410888617985 |