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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Main Authors: Zia Ud Din, Edson Rodrigues-Filho
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:Arabian Journal of Chemistry
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535216301587
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spelling 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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