1365634-18-9Relevant academic research and scientific papers
Synthesis of ketone from alkyl halide using α-chloro nitrone as oxidizing reagent: A new approach
Chakraborty, Bhaskar,Sharma, Prawin Kumar
experimental part, p. 1804 - 1812 (2012/05/20)
Consecutive SN2 reaction of α-chloronitrones were studied with isopropyl halides, and the nitrones have remarkable oxidizing properties for the conversion of isopropyl halides to ketones with good 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. Copyright Taylor & Francis Group, LLC.
New and efficient methodology of aldehyde synthesis from alkyl halide using α-chloro nitrone as a new, stable and potential oxidizing reagent
Chakraborty, Bhaskar,Sharma, Prawin Kumar,Chhetri, Manjit Singh,Kafley, Saurav,Ghosh, Aloranjan
, p. 245 - 250 (2012/04/04)
Consecutive SN2 reaction of α-chloro nitrones are studied with alkyl halides and the nitrones are found to have remarkable oxidizing properties for the conversion of alkyl halides to aldehydes with high yield. In addition, the side product obtained can serve as efficient dipolarophile in 1,3-DCR to produce spiro cycloadducts in good yields.
