ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): Jairaj K Dawle, Suryawanshi V B, S R Mathapati, A S Bondge, K I Momin

Email(s): amritkund_jk@rediffmail.com

DOI: 10.5958/0974-4150.2016.00093.6   

Address: Jairaj K Dawle1*, Suryawanshi V B2, S R Mathapati3, A S Bondge4, K I Momin5
1Reserch Lab of Pure and Applied Chemistry, Maharashtra Mahavidhyalaya, Nilanga, Dist: Latur.
2Department of Chemistry, K M C College, Khopoli, Dist Raigad.
3Department of Chemistry, S. M. P. College, Murum, Omerga, Dist: Osmanabad.
4Department of Chemistry, Shivneri Mahavidhyalaya, Shirur Anantpal, Dist Latur.
5Department of Chemistry, Rajshri Shahu Mahavidhyalaya, Latur.
*Corresponding Author

Published In:   Volume - 9,      Issue - 12,     Year - 2016


ABSTRACT:
Numerous imidazole derivatives are reported as pharmacological agents like azomycin, clotrimazole, Miconazole, ergothionine, clonidine and moxonidine. One of the most important applications of imidazoles derivatives are treatment for denture and cancer therapy. Imidazoles are in general, well known to possess, anti-cancer activity. These compounds are 5 membered planar ring, soluble in water and other polar solvents. Radziszewski and Jaapproposed the first synthesis of the imidazole corein 1882, starting from 1,2-dicarbonyl compounds, aldehydes and ammonia to obtain 2,4,5-triphenylimidazole [1, 2].


Cite this article:
Jairaj K Dawle, Suryawanshi V B, S R Mathapati, A S Bondge, K I Momin. Zinc Sulfamate Catalysed Synthesis of Trisubstituted Imidazole. Asian J. Research Chem. 2016; 9(12): 674-678. doi: 10.5958/0974-4150.2016.00093.6


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DOI: 10.5958/0974-4150 

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