Abstract

In the title compound, C14H17NO, the piperidinone and piperidine rings both adopt a chair conformation. The chiral crystals were obtained from a racemic reaction product via spontaneous resolution.

Highlights

  • In the title compound, C14H17NO, the piperidinone and piperidine rings both adopt a chair conformation

  • The chiral crystals were obtained from a racemic reaction product via spontaneous resolution

  • The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry

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Summary

Data collection

R factor = 0.043; wR factor = 0.092; data-to-parameter ratio = 15.3. C14H17NO, the piperidinone and piperidine rings both adopt a chair conformation. The chiral crystals were obtained from a racemic reaction product via spontaneous resolution

Related literature
Agilent Xcalibur Eos diffractometer
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