Use of residual dipolar couplings in conformational analysis of meta-disubstituted calix[4]arenes
Status PubMed-not-MEDLINE Language English Country England, Great Britain Media print
Document type Journal Article
PubMed
24820209
DOI
10.1039/c4cc02274b
Knihovny.cz E-resources
- Publication type
- Journal Article MeSH
Dimercuration of tetrapropoxy calix[4]arene followed by a reaction with isoamyl nitrite afforded dinitroso regioisomers with unique substitution patterns. The unusual conformational behaviour of these inherently chiral systems was revealed by the combination of dynamic NMR and residual dipolar coupling (RDC) techniques.
References provided by Crossref.org
Enantiodiscrimination of Inherently Chiral Thiacalixarenes by Residual Dipolar Couplings