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      On the origins of triterpenoid skeletal diversity

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      Phytochemistry
      Elsevier BV

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          Abstract

          The triterpenoids are a large group of natural products derived from C(30) precursors. Nearly 200 different triterpene skeletons are known from natural sources or enzymatic reactions that are structurally consistent with being cyclization products of squalene, oxidosqualene, or bis-oxidosqualene. This review categorizes each of these structures and provides mechanisms for their formation.

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          Author and article information

          Journal
          Phytochemistry
          Phytochemistry
          Elsevier BV
          00319422
          February 2004
          February 2004
          : 65
          : 3
          : 261-291
          Article
          10.1016/j.phytochem.2003.11.014
          14751299
          b3d7b91b-443b-4de5-b0e8-deb019a7a35f
          © 2004

          https://www.elsevier.com/tdm/userlicense/1.0/

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