Total synthesis and stereochemical reassignment of maedamide

研究成果: Article

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Abstract The first total synthesis of maedamide, an acyclic peptide isolated from a marine cyanobacterial assemblage of Lyngbya sp., was achieved. This synthesis led to reassignment of the allo-d-Ile of maedamide to be l-Ile, which was supported by <sup>1</sup>H and <sup>13</sup>C NMR data.

元の言語English
記事番号46482
ページ(範囲)4947-4949
ページ数3
ジャーナルTetrahedron Letters
56
発行部数34
DOI
出版物ステータスPublished - 2015 5 29

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ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

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