Biosynthesis of the alkyl group at C-24 of poriferasterol and Δ5-ergostenol in Chlorella ellipsoidea
Author:
Publisher
Elsevier BV
Subject
Horticulture,Plant Science,Molecular Biology,General Medicine,Biochemistry
Reference11 articles.
1. Some problems concerning biological C-alkylation reactions and phytosterol biosynthesis
2. Studies on the Mechanism of Biological Carbon Alkylation Reactions*
3. The Synthesis of Labelled 24-Methylenelanosterol and its Conversion into Ergosterol
4. Fucosterol Reduction to Clionasterol in vivo by Chlorella ellipsoidea
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1. Mechanism of clerosterol biosynthesis in Ajuga hairy roots: stereochemistry of C-28 methylation of 24-methylene sterol;Tetrahedron Letters;2002-07
2. Biosynthesis of campesterol and dihydrobrassicasterol in cultured cells of Amsonia elliptica;Phytochemistry;1992-05
3. 24β-Ethylsterol biosynthesis: Incorporation of l-[ME-2H3]methionine in tissue cultures of Trichosanthes kirilowii;Phytochemistry;1992-01
4. The Biosynthesis of Ergosterol;Pesticide Science;1984-04
5. The conversion of (24S)-24-ethylcholesta-5,22,25-trien-3β-ol into poriferasterol, both in vivo and with a cell-free homogenate of the alga Trebouxia sp.;Phytochemistry;1983-01
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