Print ISSN:-2394-2789

Online ISSN:-2394-2797

CODEN : IJPCN9




Downlaod Files

   


Article Access statistics

Viewed: 1752

PDF Downloaded: 1490


Synthetic trends followed for the development of 1,3,4-oxadiazole based compounds


Full Text PDF


Original Article

Author Details : Garima Verma, Mohemmed Faraz Khan, Wasim Akhtar, Mohammad Mumtaz Alam, Mohammad Shaquiquzzaman

Volume : 4, Issue : 2, Year : 2017

Article Page : 37-42


Suggest article by email

Get Permission

Abstract

1,3,4-oxadiazoles, heterocycles bearing one oxygen and two nitrogen atoms in a five membered ring have their application in the diverse areas of medicine. Enough literature is available demonstrating antibacterial, antifungal, anticonvulsant, antiviral, antidiabetic and antimalarial potential of the moiety. Owing to their wide applications, scientists across the globe are engaged in the design and development of oxadiazole derived medicinal agents. This motif can also be traced in a number of drug molecules. Most commonly adopted method for their synthesis includes he reaction between acid hydrazides and acid chorides/carboxylic acids or direct cyclization of diacylhydrazines in the presence of different dehydrating agents like phosphorus oxychloride, thionyl chloride, phosphorus pentaoxide and polyphosphoric acid. This manuscript covers different conventional and non-conventional approaches adopted for the synthesis of 1,3,4-oxadiazole derivatives.

Keywords: 1,3,4-Oxadiazole, Synthesis, Cyclization Agent, Microwave Assisted Synthesis



How to cite : Verma G, Khan M F, Akhtar W, Alam M M, Shaquiquzzaman M, Synthetic trends followed for the development of 1,3,4-oxadiazole based compounds. Int J Pharm Chem Anal 2017;4(2):37-42


This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.