First Total Synthesis of Cleroindicin B, (±) Cleroindicin C and E

Jin CHEN Jun TIAN Feng E WU Norio Kawabe Masahiko Tokuda

引用本文: Jin CHEN,  Jun TIAN,  Feng E WU,  Norio Kawabe,  Masahiko Tokuda. First Total Synthesis of Cleroindicin B, (±) Cleroindicin C and E[J]. Chinese Chemical Letters, 2001, 12(9): 771-774. shu
Citation:  Jin CHEN,  Jun TIAN,  Feng E WU,  Norio Kawabe,  Masahiko Tokuda. First Total Synthesis of Cleroindicin B, (±) Cleroindicin C and E[J]. Chinese Chemical Letters, 2001, 12(9): 771-774. shu

First Total Synthesis of Cleroindicin B, (±) Cleroindicin C and E

  • 基金项目:

    This work was financially supported by Di-Ao Science Fund, Chinese Academy of Sciences. We are grateful to Mr. F. Su and Mrs. B. R. Bai for recording the NMR spectra.

摘要: Cleroindicin B, C and E, three new natural products originally isolated from Clerodendrum indicum, have been synthesized (in racemic forms for Cleroindicin C and E) by a facile route, starting from 2-(p-methoxy-phenyl) ethanol 1. The (±) cleroindicin C (5) has been resovled by the enantioselective inclusion methodology.

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  • 收稿日期:  2001-02-22
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