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

Kirsten J Goodall; Margaret A Brimble; David Barker

doi:10.1002/mrc.2027

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

Magn Reson Chem. 2007 Aug;45(8):695-9. doi: 10.1002/mrc.2027.

Authors

Kirsten J Goodall¹, Margaret A Brimble, David Barker

Affiliation

¹ Department of Chemistry, The University of Auckland, 23 Symonds St., Auckland, New Zealand.

PMID: 17568454
DOI: 10.1002/mrc.2027

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.

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Alkanes
Bridged Bicyclo Compounds, Heterocyclic / chemistry*
Carbon Isotopes
Ligands
Magnetic Resonance Spectroscopy*
Molecular Mimicry
Molecular Structure
Polycyclic Compounds / chemistry*
Receptors, Nicotinic / metabolism
Terpenes

Substances

Alkanes
Bridged Bicyclo Compounds, Heterocyclic
Carbon Isotopes
Ligands
Polycyclic Compounds
Receptors, Nicotinic
Terpenes
nonane