S Lai, TF Zhao, XK Wang, Y Shizuri , S Yamamura, . PREPARATION AND STRUCTURAL ELUCIDATION OF INSULARINE-N-OXIDESJ. Acta Pharmaceutica Sinica, 1993, 28(7): 557-560.
Citation: S Lai, TF Zhao, XK Wang, Y Shizuri , S Yamamura, . PREPARATION AND STRUCTURAL ELUCIDATION OF INSULARINE-N-OXIDESJ. Acta Pharmaceutica Sinica, 1993, 28(7): 557-560.

PREPARATION AND STRUCTURAL ELUCIDATION OF INSULARINE-N-OXIDES

  • 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.
  • loading

Catalog

    Turn off MathJax
    Article Contents

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return