N-15 NMR and crystal structure studies of 5-(2-pyridylmethylene)-pseudothiohydantoin; dipolar dephasing experiments for establishing the preferred tautomer in the solid and solution states
Mm. Chowdhry et al., N-15 NMR and crystal structure studies of 5-(2-pyridylmethylene)-pseudothiohydantoin; dipolar dephasing experiments for establishing the preferred tautomer in the solid and solution states, J CHEM S P2, (11), 2000, pp. 2265-2268
Citations number
18
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
The preferred tautomeric form of 5-(2-pyridylmethylene)pseudothiohydantoin
1 in the solid and solution states has been determined by natural abundance
high-resolution N-15 NMR studies and by a single crystal X-ray structural
analysis.