Title of article
Stereochemistry of the reduction of 24-ethyldesmosterol to sitosterol in tissue cultures of Oryza sativa
Author/Authors
Yoshinori Fujimoto، نويسنده , , Naoko Sato، نويسنده , , Tatsuya Okuzumi، نويسنده , , Junko Yamada، نويسنده , , Masuo Morisaki، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1998
Pages
4
From page
205
To page
208
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.
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
1998
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
789211
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