CLERODANE-TYPE AND HALIMANE-TYPE DITERPENOIDS FROM THE LIVERWORT JUNGERMANNIA-HYALINA

被引:16
作者
NAGASHIMA, F
TANAKA, H
KAN, Y
HUNECK, S
ASAKAWA, Y
机构
[1] TOKUSHIMA BUNRI UNIV,FAC PHARMACEUT SCI,TOKUSHIMA 770,JAPAN
[2] INST BIOCHEM PFLANZEN,D-06120 HALLE,GERMANY
关键词
JUNGERMANNIA HYALINA; JUNGERMANNIACEAE; HEPATICAE; ENT-3-BETA; 4-BETA-EPOXYCLEROD-13E-EN-15-AL; 4-BETA-EPOXYCLEROD-13Z-EN-15-AL; KOLAVENOL; 4-BETA-EPOXYCLEROD-13E-EN-15-OL; 3R-ASTERISK; 4R-ASTERISK-DIHYDROXYCLEROD-13E-EN-15-AL; 4R-ASTERISK-DIHYDROXYCLEROD-13Z-EN-15-AL; 3-XI-HYDROXY-5(10); 13E-HALIMADIEN-15-AL; CLERODANE; HALIMANE; DITERPENOID;
D O I
10.1016/0031-9422(95)00238-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Three new clerodane- and one new halimane-type diterpenoids: ent-3 beta,4 beta-epoxyclerod-13E-en-15-ol; 3R*, 4R*-dihydroxyclerod-13E-en-15-al; 3R*, 4R*-dihydroxyclerod-13Z-en-15-al; and 3 xi-hydroxy-5(10), 13E-halimadien-15-al, were isolated from the German liverwort Jungermannia hyalina, together with the previously known clerodane-type diterpenoids ent-3 beta,4 beta-epoxyclerod-13Z-en-15-al; ent-3 beta,4 beta-epoxyclerod-13Z-en-15-al and kolavenol. The structures were determined by extensive NMR techniques and chemical degradation.
引用
收藏
页码:209 / 212
页数:4
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