| dc.contributor.author |
Gerothanassis, I |
en |
| dc.contributor.author |
Cobb, J |
en |
| dc.contributor.author |
Kimbaris, A |
en |
| dc.contributor.author |
Smith, J |
en |
| dc.contributor.author |
Varvounis, G |
en |
| dc.date.accessioned |
2014-06-06T06:43:05Z |
|
| dc.date.available |
2014-06-06T06:43:05Z |
|
| dc.date.issued |
1996 |
en |
| dc.identifier.uri |
http://dx.doi.org/10.1016/0040-4039(96)00492-3 |
en |
| dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/997 |
|
| dc.subject |
Substituent Effect |
en |
| dc.title |
17O and 14N NMR studies of quinoxaline-2(1H),3(4H)-diones and N,N′-substituted oxamides: The first experimental evidence of torsion angle deformation resulting from an unprecedented through six-bond substituent effect on the diamide group of quinoxaline-2(1H),3(4H)-diones |
en |
| heal.type |
journalArticle |
en |
| heal.identifier.primary |
10.1016/0040-4039(96)00492-3 |
en |
| heal.publicationDate |
1996 |
en |
| heal.abstract |
17O and 14N NMR studies of quinoxaline-2(1H),3(4H)-diones demonstrate a significant torsion angle deformation of the diamide group in solution due to an unprecedented through six bond substituent effect. |
en |
| heal.journalName |
Tetrahedron Letters |
en |
| dc.identifier.doi |
10.1016/0040-4039(96)00492-3 |
en |