H-1 and C-13 NMR spectra of methylmaleimido- and methylsuccinimidoanthranilate esters of 1-hydroxymethyl-6-methoxy-3-azabicyclo[3.3.1]nonanes

Goodall, Kirsten; Brimble, Margaret; Barker, David

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