Synthesis of sphingosine relatives. Part V Synthesis of both 2,3-erythro-and 2,3-threo-isomers of aplidiasphingosine, a marine terpenoid.

DOI
  • UMEMURA Takeaki
    Department of Agricultural Chemistry, The University of Tokyo on leave from Sumitomo Chemical Co.
  • MORI Kenji
    Department of Agricultural Chemistry, The University of Tokyo

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抄録

Both 2, 3-erythro- and 2, 3-threo-isomers of aplidiasphingosine were synthesized. By examining their 13C NMR spectra, 2, 3-threo- and 13, 14-erythro-relative configurations are proposed for aplidiasphingosine.

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詳細情報 詳細情報について

  • CRID
    1390282681444726272
  • NII論文ID
    110006323125
  • NII書誌ID
    AA00515312
  • DOI
    10.1271/bbb1961.51.217
  • COI
    1:CAS:528:DyaL2sXmtlOjtLs%3D
  • ISSN
    18811280
    00021369
  • 本文言語コード
    en
  • データソース種別
    • JaLC
    • Crossref
    • CiNii Articles
  • 抄録ライセンスフラグ
    使用不可

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