Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones
Ionic liquid dimethylammonium dimethylcarbamate (DIMCARB) catalyzed reaction for the synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones has been developed. Catalytic amount of DIMCARB was used in green solvent (water and ethanol) for different reaction of cyclic and acyclic keto...
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doaj-798b025c37554593aa9bcecae3ac08042020-11-25T01:37:09ZengElsevierArabian Journal of Chemistry1878-53522019-12-0112847564763Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanonesZia Ud Din0Edson Rodrigues-Filho1Fax: +55 (016) 3351 8350.; LaBioMMi, Departamento de Química, Universidade Federal de São Carlos, CP 676, 13.565-905 São Carlos, SP, BrazilFax: +55 (016) 3351 8350.; LaBioMMi, Departamento de Química, Universidade Federal de São Carlos, CP 676, 13.565-905 São Carlos, SP, BrazilIonic liquid dimethylammonium dimethylcarbamate (DIMCARB) catalyzed reaction for the synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones has been developed. Catalytic amount of DIMCARB was used in green solvent (water and ethanol) for different reaction of cyclic and acyclic ketones with different electron donating and withdrawing substituted aldehydes. Yields were recorded from low to excellent. This synthetic methodology provides mild, efficient, and environmentally friendly access to unsymmetrical curcuminoid analogs, avoiding the use of excess catalysts, chlorinated organic solvent, and high temperature reaction. It is green and environmentally sound alternative to the existing protocols for the synthesis of pharmaceutically important unsymmetrical natural product analogs. Keywords: Monoarylidene, Diarylidene cycloalkanone, Ionic liquid, DIMCARB, Curcuminoidshttp://www.sciencedirect.com/science/article/pii/S1878535216301587 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zia Ud Din Edson Rodrigues-Filho |
spellingShingle |
Zia Ud Din Edson Rodrigues-Filho Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones Arabian Journal of Chemistry |
author_facet |
Zia Ud Din Edson Rodrigues-Filho |
author_sort |
Zia Ud Din |
title |
Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones |
title_short |
Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones |
title_full |
Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones |
title_fullStr |
Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones |
title_full_unstemmed |
Optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones |
title_sort |
optimized one-pot synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones |
publisher |
Elsevier |
series |
Arabian Journal of Chemistry |
issn |
1878-5352 |
publishDate |
2019-12-01 |
description |
Ionic liquid dimethylammonium dimethylcarbamate (DIMCARB) catalyzed reaction for the synthesis of monoarylidene and unsymmetrical diarylidene cycloalkanones has been developed. Catalytic amount of DIMCARB was used in green solvent (water and ethanol) for different reaction of cyclic and acyclic ketones with different electron donating and withdrawing substituted aldehydes. Yields were recorded from low to excellent. This synthetic methodology provides mild, efficient, and environmentally friendly access to unsymmetrical curcuminoid analogs, avoiding the use of excess catalysts, chlorinated organic solvent, and high temperature reaction. It is green and environmentally sound alternative to the existing protocols for the synthesis of pharmaceutically important unsymmetrical natural product analogs. Keywords: Monoarylidene, Diarylidene cycloalkanone, Ionic liquid, DIMCARB, Curcuminoids |
url |
http://www.sciencedirect.com/science/article/pii/S1878535216301587 |
work_keys_str_mv |
AT ziauddin optimizedonepotsynthesisofmonoarylideneandunsymmetricaldiarylidenecycloalkanones AT edsonrodriguesfilho optimizedonepotsynthesisofmonoarylideneandunsymmetricaldiarylidenecycloalkanones |
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1725059335070941184 |