Studies of 13C NMR spectra of 13C-enriched cycloartenol biosynthesized from [1-13C]-, [2-13C]-and [1,2-13C2]-acetate. Revised 13C NMR spectral assignments of cycloartenol and cycloartanol and 13C NMR spectral support for the generally accepted skeleton formation mechanism of cycloartenol
β Scribed by Wasuke Kamisak; Chie Honda; Kiyoko Suwa; Koichiro Isoi
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 409 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
β¦ Synopsis
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-
π SIMILAR VOLUMES
## One-bond and long-range two-dimensional 'H-I'C NMR experiments allow the unequivocal assignment of 13C and 'H spectra. On this basis, previous assignments of 13C signals of grossularine-1 and -2 have been revised.
A number of modified retinals and retinoic esters carrying one or two methoxy groups or one methoxy and one methyl group on the polyene chain were investigated by 'H and " C NMR spectroscopy. Spectral assignments were made from homo-and selective =C{'H} hetero-decoupling experiments and from chemica
The 17O, 13C and 1H NMR spectra of a number of 1,2-dialkoxyethenes R1OCHxCHOR2 were recorded. The O atoms, in particular those of the E forms, are strongly shielded relative to the 17O nuclei of the corresponding alkyl vinyl ethers Moreover, in compounds of the type ROCHxCHOMe, the di β er-ROCHxCH 2