| Literature DB >> 9871655 |
Y Fujimoto1, N Sato, T Okuzumi, J Yamada, M Morisaki.
Abstract
Feeding of [26-13C]- and [27-13C]-24-ethyldesmosterols to cultured cells of Oryza sativa followed by 13C-NMR analysis of the biosynthesized sitosterol revealed that the reduction of 24(25)-double bond proceeds with an anti-addition of hydrogen atoms, thus the E-methyl group of the olefinic precursor becomes the pro-S-methyl on C-25 of sitosterol.Entities:
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Year: 1998 PMID： 9871655 DOI： 10.1016/s0960-894x(97)10220-7
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN： 0960-894X Impact factor: 2.823