Die absoluté Konfiguration von Michellamin B, einem „dimeren”︁, anti‐HIV‐aktiven Naphthylisochinolin‐Alkaloid
暂无分享，去创建一个
[1] G. Bringmann,et al. Dioncoline A and its Atropisomer: “Inverse Hybrid Type” Ancistrocladaceae/Dioncophyllaceae Alkaloids from Ancistrocladus abbreviatus , 1992 .
[2] G. Bringmann,et al. Ancistrobrevine D: An Unusual Alkaloid from Ancistrocladus abbreviatus , 1992 .
[3] G. Bringmann,et al. ancistrobrevine B, the first naphthylisoquinoline alkaloid with A 5,8′-coupling site, and related compounds from Ancistrocladus abbreviatus , 1992 .
[4] G. Bringmann,et al. Ancistrobrevine C: A “Mixed” Ancistrocladaceae/Dioncophyllaceae-Type Naphthylisoquinoline Alkaloid from Ancistrocladus abbreviatus , 1991 .
[5] M. Boyd,et al. Novel alkaloids from the tropical plant Ancistrocladus abbreviatus inhibit cell killing by HIV-1 and HIV-2. , 1991, Journal of medicinal chemistry.
[6] G. Rücker,et al. Polyacetylene in den unterirdischen Teilen von Cichorium intybus , 1991 .
[7] Y. Oshima,et al. Neolignans and Lignans of Nardostachys jatamansi Roots1. , 1991, Planta medica.
[8] G. Bringmann,et al. A facile degradation procedure for determination of absolute configuration in 1,3-dimethyltetra- and dihydroisoquinolines , 1991 .
[9] G. Bringmann,et al. Dioncophylline B, a naphthylisoquinoline alkaloid with a new coupling type fromTriphyophyllum peltatum , 1991 .
[10] G. Bringmann,et al. First total synthesis of (−)-dioncophylline A (“Triphyophylline”) and of selected stereoisomers: Complete (revised) stereostructure , 1990 .