Author(s): Goyal Rupendra, Jain Suman, Agarwal D D

Email(s): goyalrk09@gmail.com

DOI: 10.52711/0974-360X.2022.00517   

Address: Goyal Rupendra1*, Jain Suman2, Agarwal D D3
1Assistant Professor, SOS in Pharmaceutical Sciences, Jiwaji University, Gwalior (M.P.)
2Director, SOS in Pharmaceutical Sciences, Jiwaji University, Gwalior (M.P.)
3Professor, SOS in Chemistry, Jiwaji University, Gwalior (M.P.)
*Corresponding Author

Published In:   Volume - 15,      Issue - 7,     Year - 2022


ABSTRACT:
Chemically, curcumin is a diaryl heptanoid, belonging to the group of curcuminoids, which are natural phenols responsible for turmeric's yellow color. It is a Keto–enol tautomer, existing in enolic form in organic solvents and in keto form in water. The one pot three component of hydrazide substituted benzaldehyde was used for the synthesis of curcumin derivatives. In this work the synthesis of curcumin derivatives was done using an environmental friendly procedure via Mg-Al-CO3 hydrotalcites which have been used as efficient catalysts. These catalysts are inexpensive and non-toxic powders. Data of Spectra and other analytical technique supported identification of compound curcumin derivatives. The present work offers many merits such as the reaction conditions were extremely simple, there was operational simplicity, reaction time was short, easy to work up and purification was also easy for the products via simple means of re-crystallization. The antibacterial activity of three compounds B2, B4 and D3 was found to be near to the significant with standard compounds amoxicillin.


Cite this article:
Goyal Rupendra, Jain Suman, Agarwal D D. Synthesis, characterization and antimicrobial study of novel substituted Curcumin Derivatives. Research Journal of Pharmacy and Technology. 2022; 15(7):3091-5. doi: 10.52711/0974-360X.2022.00517

Cite(Electronic):
Goyal Rupendra, Jain Suman, Agarwal D D. Synthesis, characterization and antimicrobial study of novel substituted Curcumin Derivatives. Research Journal of Pharmacy and Technology. 2022; 15(7):3091-5. doi: 10.52711/0974-360X.2022.00517   Available on: https://rjptonline.org/AbstractView.aspx?PID=2022-15-7-39


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