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
- 1 August 1987
- journal article
- research article
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 25 (8) , 683-687
- https://doi.org/10.1002/mrc.1260250806
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Uvariastrol, a novel cycloartane triterpene from the stem bark of Uvariastrum zenkeriPhytochemistry, 1984
- Application of biosynthetic 13C‐enrichment using [1‐13C]‐, [2‐13C]‐ and [1,2‐13C2]‐acetate as precursor for 13C NMR spectral assignment of higher plant metabolites. The assignments of some bryonolic acid derivativesMagnetic Resonance in Chemistry, 1984
- Carbon-13 NMR spectra of some tetra- and pentacyclic triterpene methyl ethersMagnetic Resonance in Chemistry, 1980
- Nuclear spin-spin coupling via nonbonded interactions. 1. Conformational and substituent effects on vicinal carbon-13-proton and carbon-13-carbon-13 coupling constantsJournal of the American Chemical Society, 1980
- Lanthanide- and aromatic solvent-induced shift effects on proton resonances in C-4-methylated steroids and tetracyclic triterpenoidsChemistry and Physics of Lipids, 1977
- Experimental and theoretical studies of vicinal carbon-13-carbon coupling constantsJournal of the American Chemical Society, 1974
- Studies in phytosterol biosynthesis. Mechanism of biosynthesis of cycloartenolBiochemical Journal, 1968
- Organic Growth Factor Requirements of Tobacco Tissue CulturesPhysiologia Plantarum, 1965