| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5420691 | Solid State Nuclear Magnetic Resonance | 2008 | 9 Pages |
Abstract
A solid-state NMR/theoretical study of the tautomerism of 4-substituted pyrazolinones was carried out in search of new desmotropes. Thus, the systematic exploration by 13C and 15N CPMAS NMR of a series of 4-acylpyrazolin-5-ones has allowed to determine their structure in the solid state and to find a new example of desmotropy that of 1-phenyl-4-acetyl-pyrazolinone.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Wolfgang Holzer, Rosa Ma Claramunt, Concepción López, Ibon Alkorta, José Elguero,