Author(s):
Kalimoddin I. Momin, Abhay S. Bondge, Vikas B. Surawanshi, Jairaj K. Dawale
Email(s):
amritkund_jk@rediffmail.com
DOI:
10.5958/0974-4150.2017.00122.5 
Address:
Kalimoddin I. Momin1, Abhay S. Bondge2, Vikas B. Surawanshi3, Jairaj K. Dawale4*
1Rajarshi ShahuMahavidhyalaya, Latur, Maharashtra-413512, India.
2Shivneri College, ShirurAnantpal, Dist. Latur, Maharashtra- -413544, India.
3Department of Chemistry, KMC College, Khopoli, Maharashtra- -410203 India.
4Research Laboratory for Pure and Applied Chemistry, M. M. College, Nilanga, Dist. Latur, MH413521, India.
*CorrespondingAuthor
Published In:
Volume - 10,
Issue - 6,
Year - 2017
ABSTRACT:
An efficient route for the synthesis of aromatic imines has been developed using simple protocol at room temperature. The synthesis was completed by using commercially available starting material. Here we synthesized fourteen imines derivatives with excellent yield. Synthesized intermediates showed potent inhibition of Mycobacterium tuberculosis. The Schiff’s bases shown drug like properties and is a good starting point for further exploration in antituberculosis drug discovery.
Cite this article:
Kalimoddin I. Momin, Abhay S. Bondge, Vikas B. Surawanshi, Jairaj K. Dawale. Catalyst Free Synthesis of Imines and their Biological Evaluation. Asian J. Research Chem. 2017; 10(6):719-724. doi: 10.5958/0974-4150.2017.00122.5
Cite(Electronic):
Kalimoddin I. Momin, Abhay S. Bondge, Vikas B. Surawanshi, Jairaj K. Dawale. Catalyst Free Synthesis of Imines and their Biological Evaluation. Asian J. Research Chem. 2017; 10(6):719-724. doi: 10.5958/0974-4150.2017.00122.5 Available on: https://ajrconline.org/AbstractView.aspx?PID=2017-10-6-2