@article{aa59a3bd44f643dc81da353f47f82a26,
title = "Stereochemistry of Hydrogen Addition to C-25 of Desmosterol by Sterol-Δ24-Reductase of Rat Liver Homogenate",
abstract = "Chemically synthesized (26)- and (27)-methyl-13C-labeled desmosterol (3, 5) were separately incubated with rat liver homogenate. 13C-NMR analysis of the incubation products indicated that the C-25 hydrogen of cholesterol was introduced from the si-face of 3 and the re-face of 5.",
keywords = "[2-C][l-(methoxycarbonyl)ethyl]triphenylphosphonium iodide, [26-C]desmosterol, [27-C]desmosterol, sterol-Δ24-reductase cholesterol biosynthesis",
author = "Tomoko Yagi and Noriko Kobayashi and Masuo Morisaki and Noriyuki Hara and Yoshinori Fujimoto",
year = "1994",
doi = "10.1248/cpb.42.680",
language = "English",
volume = "42",
pages = "680--682",
journal = "Chemical and Pharmaceutical Bulletin",
issn = "0009-2363",
publisher = "Pharmaceutical Society of Japan",
number = "3",
}