Hydroxylation of Cedrol by<i>m</i>-Chloroperbenzoic Acid. Synthesis of an Epimer of the Alleged “Senoxydene”
作者:Motoo Tori、Reiko Matsuda、Yoshinori Asakawa
DOI:10.1246/bcsj.58.2523
日期:1985.9
Cedrol was hydroxylated by m-chloroperbenzoic acid to give four tertiary alcohols and two secondary alcohols, one of which was converted into an epimer of “senoxydene” in four steps.
Biotransformation of (+)-Cedrol by plant pathogenic fungus, Glomerella cingulata
作者:Mitsuo Miyazawa、Hirokazu Nankai、Hiromu Kameoka
DOI:10.1016/0031-9422(95)00221-r
日期:1995.9
transformation of (+)-cedrol has been investigated by using plantpathogenicfungus, Glomerellacingulata. (+)-Cedrol was hydroxylated at the C-3 position, and transformed mainly to 3α-hydroxycedrol and with a smaller amount of 3β-hydroxycedrol. 3α-Hydroxycedrol was further transformed to 8-cedren-3α-ol by dehydration at the C-8 position. In addition, G. cingulata produced a small amount of 12-hydroxycedrol from