An NMR study of two known bis-indole alkaloids is described. In addition to conventional 1D NMR methods, 2D shift-correlated NMR experiments [ 1 Hx 1 H-COSY, 1 Hx 13 C-HMQC-1 J(C,H), 1 Hx 13 C-HMBC-n J(C,H) (n D 2 and 3)] and 2D 1 Hx 1 H-NOESY were used for 1 H and 13 C chemical shift assignments of
Four known triterpenoids isolated from three Brazilian plants: 1H and 13C chemical shift assignments
โ Scribed by F. P. Soares; C. A. V. Ronconi; E. V. L. da Cunha; J. M. Barbosa-Filho; M. S. da Silva; R. Braz-Filho
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 224 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
3b,19a,
acid and 7-oxofriedelin is described. In addition to conventional 1D NMR methods, 2D shiftcorrelated NMR experiments [1H ] 1H-COSY, (HETCOR and HMQC), 1H ] 13C-COSYร1J CH 1H ] 13C-(n \ 2 and 3, COLOC and HMBC)] and 2D 1H ] 1H-NOESY were used for 1H and 13C chemical COSYรnJ CH shift assignments of these triterpenoids.
๐ SIMILAR VOLUMES
An NMR study of 3ห-and 3ห-friedelinol is described. In addition to conventional 1D NMR methods, 2D shift-correlated NMR experiments HMQC [( 1 J(C,H)], HMBC [ n J(C,H); n D 2 and 3] and 2D 1 H, 1 H-NOESY were used for 1 H and 13 C chemical shift assignments of these triterpenes.
## Abstract Four triterpenoid saponins were isolated from Albizziae cortex, and a complete assignment of their ^1^H and ^13^C NMR spectra was carried out using 1D and 2D NMR (^1^H๏ฃฟ^1^H COSY, HSQC, HMBC, and HSQCโTOCSY) methods. Their ^1^H NMR assignments were reported for the first time and some of
## Abstract The phytochemical investigation of carnauba wax led to the isolation of three new dammarane triterpenoids 1, 2 and 4, together with the known triterpene 3. The structures of the new compounds were determined by 1D and 2D NMR spectroscopy and by comparison with published data for closely
## Abstract ^1^H and ^13^C NMR assignments of the two isomeric epoxysitosterols, 5,6ฮฑโepoxyโ5ฮฑโstigmastanโ3ฮฒโol (1) and 5,6ฮฒโepoxyโ5ฮฒโstigmastanโ3ฮฒโol (2), isolated from the leaves of __Rhododendron formosanum__ Hemsl were achieved by 1D and 2D techniques such as DEPT, HMBC, HMQC, COSY and NOESY. C