dc.contributor.author |
Goodall, Kirsten |
en |
dc.contributor.author |
Brimble, Margaret |
en |
dc.contributor.author |
Barker, David |
en |
dc.date.accessioned |
2011-09-19T02:23:47Z |
en |
dc.date.issued |
2007 |
en |
dc.identifier.citation |
Magn Reson Chem 45(8):695-699 Aug 2007 |
en |
dc.identifier.issn |
0749-1581 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/8092 |
en |
dc.description.abstract |
The 1H and 13C NMR data for 3-azabicyclo[3.3.1]nonanes having C-1 methylsuccinimidoanthranilate esters and C-6 methyl ethers were measured and assigned using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this with previously published data illustrates the effects of stereochemistry and substitution on the basic heterocyclic framework. |
en |
dc.language |
EN |
en |
dc.publisher |
John Wiley & Sons, Ltd. |
en |
dc.relation.ispartofseries |
Magnetic Resonance in Chemistry |
en |
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/0749-1581/ |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
en |
dc.subject |
NMR |
en |
dc.subject |
H-1 NMR |
en |
dc.subject |
C-13 NMR |
en |
dc.subject |
Delphinium alkaloids |
en |
dc.subject |
methylsuccinimidoanthranilate |
en |
dc.subject |
3-azabicyclo[3.3.1]nonane |
en |
dc.subject |
substituent effects |
en |
dc.subject |
stereochemistry |
en |
dc.subject |
RING-E ANALOGS |
en |
dc.subject |
NICOTINIC ACETYLCHOLINE-RECEPTORS |
en |
dc.subject |
MOLECULAR-MECHANICS CALCULATIONS |
en |
dc.subject |
ALKALOID METHYLLYCACONITINE |
en |
dc.subject |
SPECTROSCOPY |
en |
dc.subject |
ANTAGONISTS |
en |
dc.subject |
ACID |
en |
dc.title |
H-1 and C-13 NMR spectra of methylmaleimido- and methylsuccinimidoanthranilate esters of 1-hydroxymethyl-6-methoxy-3-azabicyclo[3.3.1]nonanes |
en |
dc.type |
Journal Article |
en |
dc.identifier.doi |
10.1002/mrc.2027 |
en |
pubs.issue |
8 |
en |
pubs.begin-page |
695 |
en |
pubs.volume |
45 |
en |
dc.rights.holder |
Copyright: 2007 John Wiley & Sons, Ltd. |
en |
dc.identifier.pmid |
17568454 |
en |
pubs.end-page |
699 |
en |
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
en |
pubs.subtype |
Article |
en |
pubs.elements-id |
74020 |
en |
pubs.org-id |
Science |
en |
pubs.org-id |
Chemistry |
en |
pubs.org-id |
Science Research |
en |
pubs.org-id |
Maurice Wilkins Centre (2010-2014) |
en |
pubs.record-created-at-source-date |
2010-09-01 |
en |
pubs.dimensions-id |
17568454 |
en |