Author(s): B. R. Thorat, M. Mustapha, D. Khandekar, Swati Lele, P. Kamat, S. Sawant, R. Jadhav, D. Shelke, Shivaji Kolekar, R. G. Atram, R. Yamgar

Email(s): devs_mdu@yahoo.com

DOI: Not Available

Address: B. R. Thorat, M. Mustapha, D. Khandekar, Swati Lele, P. Kamat, S. Sawant, R. Jadhav, D. Shelke, Shivaji Kolekar, R. G. Atram and R. Yamgar
P. G. Dept of Chemistry, Govt. of Maharashtra, Ismail Yusuf College of Arts, Science and Commerce, Jogeshwari (East), Mumbai 400 060.
*Corresponding Author

Published In:   Volume - 5,      Issue - 3,     Year - 2012


ABSTRACT:
A simple and regioselective synthesis of 2-chloro-3-formylquinoline [1] by the cyclisation of N-aryacetamide has been reported by the Vilsmeier Haack reaction/cyclisation. 2-Chloro-3-formylquinoline, the formyl group shows condensation with variety of haloanilines & hydrazones and forming schiff bases N-[(E)-(2-chloroquinolin-3-yl)methylidene]anilides [2a-e] which are further subjected to fluorescence study.


Cite this article:
B. R. Thorat, M. Mustapha, D. Khandekar, Swati Lele, P. Kamat, S. Sawant, R. Jadhav, D. Shelke, Shivaji Kolekar, R. G. Atram, R. Yamgar. Synthesis and Fluorescence Properties of Schiff Bases of 2-chloro-3-formylquinoline. Research J. Pharm. and Tech. 5(3): March 2012; Page 369-375.


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