## Abstract The ^1^H and ^13^C NMR data for 3โazabicyclo[3.3.1]nonanes with OH and OMe substituents at Cโ6 and Cโ9 were measured using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this NMR data illustrates the effects of stereochemistry and substitution at these positions.
1H and 13C NMR data for C-6 substituted 3-azabicyclo[3.3.1]nonane-1-carboxylates
โ Scribed by Kirsten J. Goodall; Margaret A. Brimble; David Barker
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 122 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1878
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โฆ Synopsis
Abstract
The ^1^H and ^13^C NMR spectra of 3โazabicyclo[3.3.1]nonanes with various oxygenated substituents at Cโ6 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 Cโ6 in these compounds. Copyright ยฉ 2006 John Wiley & Sons, Ltd.
๐ SIMILAR VOLUMES
## Abstract The ^13^C NMR spectra of 26 substituted 2โazabicyclo[3.3.1]nonanโ7โones are reported, providing a diagnostic method for the stereochemical elucidation of the relative configuration of these products.
## Abstract The ^1^H and ^13^C NMR data for 3โazabicyclo[3.3.1]nonanes having Cโ1 methylsuccinimidoanthranilate esters and Cโ6 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 eff
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