The assignments of 13C and 1H NMR spectra for madeirane triterpenes are reported. The assignments were made on the basis of two-dimensional homonuclear 1H, 1H (COSY) and of 1H detected 1H, 13C heteronuclear correlation (HMQC) and also from a series of one-dimensional selective INEPT experiments. 19
Carbon-13 nuclear magnetic resonance spectra of exo- and endo-2-norbornyltrimethyl-stannanes: Corrected assignments
✍ Scribed by William Kitching
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 152 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C NMR spectra of pure exo‐2‐norbornyltrimethylstannane and a mixture of the exo‐ and endo‐isomers have been recorded. ^1^H–^13^C polarization transfer spectra have been obtained and require the previously reported assignments for C‐3 and C‐4 in the exo‐isomer to be reversed. The reported assignments for the endo‐isomer are correct. The new assignment for C‐4‐exo [with J(^119^Sn,^13^C) vic=12 Hz, instead of the previously assigned J(vic)=23 Hz], has a very minor effect on the nature of the Karplus curve [for ^3^J(^119^Sn,^13^C)] generated previously.
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