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Title: Structural revision of four spiramine diterpenoid alkaloids from the roots of Spiraea japonica. Author: Wang BG, Hong X, Zuo GY, Hao XJ. Journal: J Asian Nat Prod Res; 2000; 2(4):271-81. PubMed ID: 11249609. Abstract: On the basis of detailed 1H-NMR 13C-NMR spectral analysis, especially by 2D NMR experiments (1H-1H COSY, HMQC, HMBC, and NOESY) as well as by chemical transformations. four isoatisine type diterpenoid alkaloids, spiramines P and Q, and U and T, have been reassigned as the 6beta hydroxyl and 6beta acetoxyl substituents, respectively, rather than the previously assigned 15alpha counterparts in our further studies on chemical constituents of the roots of Spiraea japonica var. acuta.[Abstract] [Full Text] [Related] [New Search]