## Abstract The ^1^H and ^13^C NMR data for 3‐azabicyclo[3.3.1]nonanes with OH and OMe substituents at C‐6 and C‐9 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.
3,6,9-trioxanthracenes and 3,6-dioxa-9-thianthracenes: Conformational analysis and complete assignment of 13C NMR spectra
✍ Scribed by Marcial Moreno-Mañas; Jordi Ribas; Francisco Sánchez-Ferrando; Albert Virgili
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 172 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 20.15 MHz 13C NMR spectra of five 3,6,9-trioxanthracenes and four 3,6-dioxa-9-thianthracenes have been assigned using a variety of one-dimensional techniques. These include spin-echo multiplicity sorting (SEFT), long-range heteronuclear coupling constant determination via gated decoupling and selective heteronuclear 13C{ 'H} NOE difference spectroscopy. The axial position of substituents on C-10 has been demonstrated.
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