Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1405931 | Journal of Molecular Structure | 2012 | 10 Pages |
Abstract
⺠The new piperidin-4-one adopts chair conformation with equatorial substituents. ⺠The N-benzylpiperidin-4-ones are also in the chair conformation with equatorial substituents. ⺠The highly crowded 3,5-dialkylcompounds also adopt similar stereochemistry of 3-alkyl analogs. ⺠The N-benzylation significantly changed the chemical shifts but no conformational changes. ⺠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
Authors
Someshwar D. Dindulkar, Paramasivam Parthiban, Vedavati G. Puranik, Yeon Tae Jeong,