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

Citation
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
ISSN journal
14701820 → ACNP
Issue
11
Year of publication
2000
Pages
2265 - 2268
Database
ISI
SICI code
1470-1820(2000):11<2265:NNACSS>2.0.ZU;2-Z
Abstract
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.