ISSN

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


Author(s): Laxmi Lal Dangi, Mangal S. Dulawat, Parul Tiwari, Shiv Singh Dulawat

Email(s): Email ID Not Available

DOI: Not Available

Address: Laxmi Lal Dangi1*, Mangal S. Dulawat1, Parul Tiwari1 and Shiv Singh Dulawat2
Department of Chemistry, B.N.P.G. College, M.L.Sukhadia University, Udaipur-313001 (Raj.) India
*Corresponding Author

Published In:   Volume - 6,      Issue - 5,     Year - 2013


ABSTRACT:
Chalcones represent a group of compounds with interesting biological activities that are formed from a Claisen-Schmidt condensation between a aromatic benzaldehyde and an acetophenones in the presence of sodium hydroxide NaOH as a catalyst. A m-phenoxy benzaldehyde reacted with substituted aromatic acetophenones in presence of base to formed chalcones. The structures of all the synthesized compounds have been confirmed by elemental analysis and spectral data. The synthesized compounds have been tested for their antifungal activity.


Cite this article:
Laxmi Lal Dangi, Mangal S. Dulawat, Parul Tiwari, Shiv Singh Dulawat. New substituted m-Phenoxy chalcones; their synthesis by microwave irradiation and antifungal activity. Asian J. Research Chem. 6(5): May 2013; Page 461-463.


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