Organic Chemistry laboratory, Sikkim Government College, Gangtok, Sikkim- 737102, India
*Corresponding Author E-mail: bhaskargtk@yahoo.com
Online published on 6 March, 2013.
Consecutive SN2 reaction of α-chloro nitrones are studied with isopropyl halides and the nitrones are found to have remarkable oxidizing properties for the conversion of isopropyl halides to ketones with high yields. In addition, the side product obtained can serve as efficient dipolarophile in 1,3-Dipolar cycloaddition reaction to produce spiro cycloadduct in good yield.
α-chloro nitrone, ketone synthesis, reusable side product