An Efficient Method for the Synthesis of Nitropiperidones
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A three step efficient strategy for the synthesis of substituted5-nitropiperidones in high de, employing Michael additionof N-p-tolylsulfinyl fchars/beta2.gif" BORDER=0 ALIGN="middle">-nitroamines to fchars/alpha.gif" BORDER=0>,fchars/beta2.gif" BORDER=0 ALIGN="middle">-unsaturated esters,hydrolysis of the sulfinyl group, and cyclization of theresulting free amines, has been developed. A very simpleexperimental procedure involving mild conditions and onlyone chromatographic purification are the main features ofthe process.

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