ISSN

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


Author(s): Bhaskar Chakraborty, Prawin K. Sharma

Email(s): bhaskargtk@yahoo.com

DOI: Not Available

Address: Bhaskar Chakraborty* and Prawin K. Sharma
Organic Chemistry laboratory, Sikkim Government College, Gangtok, Sikkim 737102, India
*Corresponding Author

Published In:   Volume - 4,      Issue - 1,     Year - 2011


ABSTRACT:
Consecutive SN2 reaction of a-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.


Cite this article:
Bhaskar Chakraborty, Prawin K. Sharma. New and Efficient Route for the Synthesis of Ketone from Alkyl Halide Using α-Chloro Nitrone as Oxidizing Reagent. Asian J. Research Chem. 4(1): January 2011; Page 95-99.


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RNI: Not Available                     
DOI: 10.5958/0974-4150 

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