Comparison of the behavior of oxidosqualene cyclases from pig liver and yeast toward epoxy-squalene analogues possessing a Δ 18–19 Z or E C, C Double bond.
暂无分享,去创建一个
[1] G. Prestwich,et al. Vinyl oxirane analog of (3S)-2,3-epoxysqualene: A substrate for oxldosqualene cyclases from yeast and from hog liver , 1990 .
[2] J. Medina,et al. Vinyl group rearrangement in the enzymic cyclization of squalenoids: synthesis of 30-oxysterols , 1989 .
[3] J. Medina,et al. Enzymic cyclization of hydroxylated surrogate squalenoids with bakers' yeast , 1988 .
[4] K. Kyler,et al. Enantioselective enzymic sterol synthesis by ultrasonically stimulated bakers' yeast , 1988 .
[5] E. Guittet,et al. About the mechanism of sterol biosynthesis , 1987 .
[6] C. Djerassi. Recent studies in the marine sterol field , 1981 .
[7] A. Burlingame,et al. Enzymic cyclization of trans,trans,trans-18,19-dihydrosqualene 2,3-oxide. , 1967, Journal of the American Chemical Society.