1-alkynyldioxaborolanes: Determination of 1J(13C,11B) from 13C NMR studies at 102°C
✍ Scribed by Bruce Victor Cheesman; Laurent Deloux; Morris Srebnik
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 449 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Broad ^13^C resonances, as the result of partially relaxed scalar ^13^C^11^B coupling, were observed for the C‐1 and to a lesser extent C‐2 carbons of 1‐alkynyldioxaborolanes at 25°C. Measurement of the ^13^C spectra at 102°C resulted in a slower ^11^B quadrupolar relaxation rate and allowed the determination of ^1^J(^13^C,^11^B) scalar coupling from the resulting quadruplets for the C‐1 carbon.
📜 SIMILAR VOLUMES
## Abstract The ^13^C NMR spectra of a series of 1‐substituted imidazoles were measured and assigned on the basis of substituent chemical shifts and ^13^C/^1^H shift correlated spectra.
Previously proposed I3C NMR spectral assignments of cycloartenol(9,19-cyclolanost-24-en-3j?-ol) (1) and cycloartanol(9,19-cyclolanostan-3/3-ol) (2) were re-examined by means of 13C-enrichment experiments and LIS measurement of "C chemical shifts. Revised signal assignments are proposed for C-
C and in some cases also 15 N chemical shifts of quaternary benzo[c]phenanthridine alkaloids (fagaronine, chelerythrine, chelilutine, chelirubine, nitidine, sanguilutine, sanguinarine, and sanguirubine) were systematically studied by NMR spectroscopy and ab initio calculations. The assignment of sig
## Abstract The ^1^H and ^13^C NMR spectra of magainin 1, a sterilizing agent of the skin, were studied using two‐dimensional techniques. All the ^1^H and ^13^C NMR resonances were unambiguously determined from a combination of 2D homo‐ and heteronuclear NMR spectroscopy.