## Abstract The ^1^H and ^13^C NMR spectra of 3‐azabicyclo[3.3.1]nonanes with various oxygenated substituents at C‐6 were assigned using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Close examination of this NMR data details the effects of substitution and stereochemistry at C‐6 in these
1H and 13C NMR spectra of methylmaleimido- and methylsuccinimidoanthranilate esters of 1-hydroxymethyl-6-methoxy-3-azabicyclo[3.3.1]nonanes
✍ Scribed by Kirsten J. Goodall; Margaret A. Brimble; David Barker
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 146 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2027
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✦ Synopsis
Abstract
The ^1^H and ^13^C 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. Copyright © 2007 John Wiley & Sons, Ltd.
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