Synthesis of the reported structure of piperazirum using a nitro-Mannich reaction as the key stereochemical determining step
James C. Anderson, Andreas S. Kalogirou, Michael J. Porter and 1 more
Beilstein Journal of Organic Chemistry · 2013
doi:10.3762/bjoc.9.200 (opens in a new tab)
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Abstract
Piperazirum, isolated from Arum palaestinum Boiss, was originally assigned as r-3,c-5-diisobutyl-c-6-isopropylpiperazin-2-one. The reported structure was synthesised diastereoselectively using a key nitro-Mannich reaction to set up the C5/C6 relative stereochemistry. The structure was unambiguously assigned by single crystal X-ray diffraction but the spectroscopic data did not match those reported for the natural product. The structure of the natural product must therefore be revised.
Abstract licence: CC BY
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