Title : Green chemistry protocol for the synthesis of some new scaffolds of isoxazolidine & isoxazoline derivatives via 1,3-dipolar cycloaddition reaction and potential biological activities of the cycloadducts
Abstract:
One of the excellent examples of spin trapping reagents is nitrones which plays fundamental role in the synthesis of five-membered heterocyclic ring compounds (commonly called isoxazolidine and isoxazoline derivatives) via 1,3-dipolar cycloaddition reactions which are an integral part of many natural products. The medicinal activities of these heterocyclic compounds always finds a tremendous interest to the synthetic organic chemists as they found to exhibit antibacterial, anticonvulsant, antibiotic, antituberculer, antifungal and anticancer activities.Except green chemistry methodologies, majority of the reported procedures for the synthesis of isoxazolidine and isoxazoline derivatives require drastic experimental conditions like high temperature and long reaction times. In addition, these reactions found to suffer from selectivity and also there are possibilities of poor yields as well as development of side products.Majority of these conventional procedures for the synthesis of isoxazolidine and isoxazoline derivatives are replaced successfully nowadays with the inception of green chemistry procedures like mechanochemistry (solid phase reaction), reactions conducted “in water” & “on water”, microwave induced reactions and many more techniques. In the present work, few excellent examples based on stereoselective 1,3-Dipolar cycloaddition reactions using green chemistry protocols have been reported. Good to excellent yields, minimum reaction time, fast & simple isolation of products, environment friendly reaction conditions and stereoselectivities in the reported reactions will certainly attract researchers working in this domain.
Keywords: Stereoselective 1,3-Dipolar cycloaddition reaction, New approaches, Green chemistry methodologies, Anticancer activity