A pulse sequence for obtaining 13C-lH shift-correlated spectra with full 'H-'H decoupling b described and evaluated. It is concluded that the sequence provides excellent resolution, even for strongly coupled methylene group The sensitivity is superior to those of existing sequences based on "C detec
Evaluation of pulse sequences combining 13C-1H shift correlation and heteronuclear J spectroscopy with full 1H-1H decoupling
✍ Scribed by Marion Perpick-Dumont; William F. Reynolds; Raúl G. Enríquez
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 616 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Three different two-dimensional "C-'H shift-correlation sequences which detect 'H chemical shifts and one bond
'3C-'H[J(CH)I couplings in f, with full 'H-'H decoupling are described and evaluated. They are particularly useful for detecting small differences in 'J(CH) for nonquivalent methylene groups in natural products and other complex organic molecules. The best of the three allows determination of 'J(CH) and 'H chemical shifts to a precision better than 1 Hz, with sensitivity comparable to previous shift-correlation and J-resolved pulse sequences. 'J(CH) Values for a typical alkaloid suggest that these parameters are a useful probe of conformational, electronic and ring size effects in natural products.
📜 SIMILAR VOLUMES
## Abstract Several different versions of the ^13^C‐detected ^13^C^1^H shift correlation sequence in phase sensitive mode with partial and full ^1^H^1^H decoupling are described and evaluated. As expected, they show sensitivity advantages over their absolute value analogues. Further, it is possib
The magnitudes and relative signs of 13C-'% and 'H-'% coupling constants in 6-F-indole, 5-and 6-F-tryptamine, 5-F-indole-3-carboxaldehyde, 2and 4-F-biphenyl, droperidol, flusperilene, l-F-naphthalene and 3-F-fluroanthene (F = fluoro) have been determined using two-dimensional % -' H chemical shift c