Studies on the alkaloids of Erythrina plants

被引:11
作者
Ito, K [1 ]
机构
[1] Meijo Univ, Fac Pharm, Tempa Ku, Nagoya, Aichi 4688503, Japan
来源
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN | 1999年 / 119卷 / 05期
关键词
erythrina alkaloid; oxo-erythrinan alkaloid; total synthesis; Birch reduction; aza-tricyclo[3.2.0.0] compound; cyclopropane;
D O I
10.1248/yakushi1947.119.5_340
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The alkaloidal components of eight Erythrina plants (Leguminosae), E. arborescence Roxb., E. orientalis (L.) MURR, E. crysta-galli LINN, E. crysta-galli (L.) cv. Maruba Deiko H. Murata, E. x bidwilli LINDL, E. poeppigiana (Walp) O. F. Cook, E. glauca WILLD, and E. variegata L. were examined. As a result of this study, five new oxo-erythrinan alkaloids, erythrinine (8), 11-hydroxyerysotrine (9), erysotramidine (10), erytharbine (11), crystamidine (12) and a di-benz[d,f]azonine type alkaloid, erybidine (2), were isolated respectively. Two tetrahydroprotoberberine type alkaloids, scoulerine (4) and coreximine (5), were also isolated from E. orientalis (L.) MURR. A new synthetic route to erythrinan alkaloids was developed, via the cia -C/D-ring fused 15-methoxy-16-hydroxyerythrinan-2, 8-dione (49) as a key intermediate, from the enol methyl derivative (48) which was obtained by Birch reduction of the benzyl amide (47). The total synthesis of (+/-)-erysotramidine (10), an oxo-erythrinan alkaloid, including a novel ring cleavage of the azatricyclo[3.2.0.0] compound (70) with phenylselenyl chloride is described.
引用
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页码:340 / 356
页数:17
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