## Abstract Several different versions of the ^13^Cโdetected ^13^C๏ฃฟ^1^H shift correlation sequence in phase sensitive mode with partial and full ^1^H๏ฃฟ^1^H decoupling are described and evaluated. As expected, they show sensitivity advantages over their absolute value analogues. Further, it is possib
Comparison of 13C Resolution and Sensitivity of HSQC and HMQC Sequences and Application of HSQC-Based Sequences to the Total 1H and 13C Spectral Assignment of Clionasterol
โ Scribed by William F. Reynolds; Stewart McLean; Li-Lin Tay; Margaret Yu; Raul G. Enriquez; Dionne M. Estwick; Keith O. Pascoe
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 488 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
It is demonstrated that HSQC gives considerably better 13C resolution and sensitivity than HMQC for CH 2 groups of natural products, particularly when combined with linear prediction. Similarly, coupled HSQC spectra provide a useful method for the determination of 1H multiplet structure and consequent assignment of individual protons as axial or equatorial in fused cyclohexane rings. These and related techniques are used to assign 1H CH 2 and 13C spectra of the marine sterol clionasterol.
๐ SIMILAR VOLUMES
Order parameters describing conformational exchange processes on the nanosecond to microsecond timescale can be obtained from powder patterns in solid-state NMR (SSNMR) experiments. Extensions of these experiments to magic-angle spinning (MAS) based high-resolution experiments have been demonstrated
The sensitivity limits for 13C-detected 13C-1H shift correlation sequences were evaluated using a microprobe in combination with 3 mm microtubes รtted with susceptibility plugs which allow for further restriction of the sample volume. For an absolute value BIRD-decoupled HETCOR spectrum acquired in
## Abstract Proton and carbon chemical shift data and protonโproton coupling constants of the synthetic antithrombotic pentasaccharide SanOrg34006 and its synthetic precursors are reported. Longโrange heteronuclear correlation experiments allow the determination of the substitution pattern of the p
## Abstract A mixture of two slowly interconverting isomeric compounds was isolated from __Bernardia laurentii__ and identified as the __trans__โ and __cisโp__โhydroxycinnamoyl esters of the triterpene taraxerol. Their ^13^C and ^1^H NMR spectra were totally assigned with the aid of concerted twoโd