The Journal of Organic Chemistry

Subsessiline: structure revision and synthesis

JW Skiles, MP Cava

文献索引：Skiles,J.W.; Cava,M.P. Journal of Organic Chemistry, 1979 , vol. 44, # 3 p. 409 - 412

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被引用次数: 24

摘要

Of the more than 20 known oxoaporphine alkaloids, only a few are phenolic in nature.'Among these, subsessiline, which has been assigned structure contains the unusual feature of a phenolic function at the C3 position of the aporphine system. In connection with other alkaloid structural studies in progress in our laboratory, we have now synthesized 9- hydroxy-1, 2, 3-trimethoxy-7H-dibenzo [de, g] quinolin-7-one