Publication: Determination of the Relative Configuration of -Amino Acid Esters Based on Residual Dipolar Couplings
| dc.bibliographiccitation.firstpage | 6801 | |
| dc.bibliographiccitation.issue | 31 | |
| dc.bibliographiccitation.journal | European Journal of Organic Chemistry | |
| dc.bibliographiccitation.lastpage | 6805 | |
| dc.contributor.author | Niklas, Thomas | |
| dc.contributor.author | Steinmetzger, Christian | |
| dc.contributor.author | Liu, Weiping | |
| dc.contributor.author | Zell, Daniel | |
| dc.contributor.author | Stalke, Dietmar | |
| dc.contributor.author | Ackermann, Lutz | |
| dc.contributor.author | John, Michael | |
| dc.date.accessioned | 2018-11-07T09:50:50Z | |
| dc.date.available | 2018-11-07T09:50:50Z | |
| dc.date.issued | 2015 | |
| dc.description.abstract | Configurational and conformational characterization of two synthetic -amino acid esters comprising an indan motif was achieved by residual dipolar couplings. We further observed that the stability of Q factors upon addition of structural noise substantially facilitates the selection of the correct structure. The two analyzed compounds differ by a single methyl group, which leads to a remarkable conformational change. | |
| dc.description.sponsorship | Studienstiftung des Deutschen Volkes | |
| dc.identifier.doi | 10.1002/ejoc.201500941 | |
| dc.identifier.isi | 000363485200002 | |
| dc.identifier.uri | https://resolver.sub.uni-goettingen.de/purl?gro-2/35787 | |
| dc.notes.status | zu prüfen | |
| dc.notes.submitter | Najko | |
| dc.publisher | Wiley-v C H Verlag Gmbh | |
| dc.relation.issn | 1099-0690 | |
| dc.relation.issn | 1434-193X | |
| dc.title | Determination of the Relative Configuration of -Amino Acid Esters Based on Residual Dipolar Couplings | |
| dc.type | journal_article | |
| dc.type.internalPublication | yes | |
| dc.type.peerReviewed | yes | |
| dc.type.status | published | |
| dspace.entity.type | Publication |