Article ID Journal Published Year Pages File Type
1405931 Journal of Molecular Structure 2012 10 Pages PDF
Abstract
► The new piperidin-4-one adopts chair conformation with equatorial substituents. ► The N-benzylpiperidin-4-ones are also in the chair conformation with equatorial substituents. ► The highly crowded 3,5-dialkylcompounds also adopt similar stereochemistry of 3-alkyl analogs. ► The N-benzylation significantly changed the chemical shifts but no conformational changes. ► The N-benzylpiperidin-4-ones exist in the chair form in solid state as well, witnessed by XRD.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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