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A three step e
fficient strategy
for the synthesis o
f substituted5-nitropiperidones in high
de, employing Michael additiono
f N-
p-tolylsul
finyl
![](/images/gi<font color=)
fchars/beta2.gi
f" BORDER=0 ALIGN="middle">-nitroamines to
![](/images/gi<font color=)
fchars/alpha.gi
f" BORDER=0>,
![](/images/gi<font color=)
fchars/beta2.gi
f" BORDER=0 ALIGN="middle">-unsaturated esters,hydrolysis o
f the sul
finyl group, and cyclization o
f theresulting
free amines, has been
developed. A very simpleexperimental procedure involving mild conditions and onlyone chromatographic puri
fication are the main
features o
fthe process.