Abstract
The furanone structure, a significant group of heterocyclic compounds, is frequently
found in natural products that are exhibiting striking pharmacological effects and
a growing field of research. They have a wide spectrum of pharmaceutical activity: anticataract,
anticancer, antibacterial, anti-inflammatory, anticonvulsant. This review article
presents a summary of natural furanones, synthetic methods, and the biological effects of
these important compounds. Solid-phase method, cross-coupling reactions, Maillard-type
reaction, the cycloaddition of alcohol and phenyl nitrile oxide, and side-chain modifications
are some types of reactions for the preparation of furanone derivatives. Methods of
preparation and pharmacological activities of furanone skeletons that are discussed in this
review article will help the medicinal chemists to design and execute novel procedures
towards finding new drugs.
Keywords:
Heterocyclic, Furanone, Biological activity, Antimicrobial, Anticancer, Anti-cataract, Anti-inflammatory.
Graphical Abstract
[1]
Arora, P.; Arora, V.; Lamba, H.; Wadhwa, D. Importance of heterocyclic chemistry: A review. Int. J. Pharm. Sci. Res., 2012, 3, 2947-2957.
[2]
Buntrock, R.E. The ACS Style Guide: Effective Communication of Scientific Information Edited by Anne M. Coghill and Lorrin R. Garson. American Chemical Society and Oxford University Press: Washington, DC and Oxford, UK 2006. ACS Publications., 2007.
[12]
Hashem, A.I.; Abou-Elmagd, W.S.; Abd-Elaziz, A. Synthesis and reactions of some 2 (3H)-and 2 (5H)-furanone. Eur. Chem. Bull., 2014, 3, 1064-1068.
[22]
Ramach, C.S.; Sreekumar, P.; Pillai, P.M.; Balaram, P. Synthesis and cytotoxicity studies of some furanone derivatives. Org.Chem: India. J., 2012, 8
[50]
Grossmann, G.; Jolivet, B.; Bornand, M.; Séquin, U.; Spindler, K-D. Synthesis and biological evaluation of some furanones as putative chitinase inhibitors. Synthesis, 2005, 2005, 1543-1549.
[65]
Ramachandran, C.S.; Sreekumar, P. Synthesis, characterisation and antibacterial evaluation of 2 (5h) furanone derivatives from highly functionalised mucobromic acid. Int. J. Pharm. Pharm. Sci., 2011, 3, 225-228.