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海岛轮环藤碱-N-氧化物的制备和结构

PREPARATION AND STRUCTURAL ELUCIDATION OF INSULARINE-N-OXIDES

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【作者】 赖盛赵同芳王宪楷志津里芳一山村庄亮

【Author】 S Lai, TF Zhao, XK Wang~*, Y Shizuri~(**) and S Yamamura~* (School of Pharmacy, West China Unirersity of Medical Sciences. Chengqdu 610041, China; ~(**) Department of Chemistry, Faculty of Science and Technology, Keio Unirersity, Iliyoshi. Yokohama 223, Japan)

【机构】 华西医科大学药学院庆应义塾大学理工学部庆应义塾大学理工学部 成都 610041成都 610041日本横滨 223日本横滨 223

【摘要】 <正> 双苄基异喹啉(BBI)生物碱在植物界分布较广,有的有较强生理活性,是一类重要异喹啉化合物。现已从13科51属植物中分得这类生物碱400余种,包括首尾氧桥型45种和尾尾氧桥型360种左右,其中N-氧化物约30种,但首尾氧桥BBI生物碱-N-氧化物迄今仅发现一种。

【Abstract】 Oxidation of insularine (Ⅰ) with m-chloroperbenzoic acid yielded four insularine-N-oxides. Two of them are identical in every respect with our insularine-2β-N-oxide (Ⅱ) and insularine-2’β-N-oxide (Ⅲ), two rare examples of naturally occurring head-to-tail bisbenzyliso-quinoline N-oxides newly isolated from Cyclea sutchnenensis, which confirmed the structures of the two novel natural N-oxides. The other two are new. compounds and their structures have been established as insularine-2’α-N-oxide (Ⅳ) and insularine-2β-2’β-N, N-dioxide (Ⅴ), on the basis of spectral data (UV, IR. ~1HNMR, NOEDS AND MS) analysis.

【基金】 国家自然科学基金
  • 【文献出处】 药学学报 ,Acta Pharmaceutica Sinica , 编辑部邮箱 ,1993年07期
  • 【下载频次】73
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