Enantioselective Synthesis of Aurilide, a Cytotoxic 26-Membered Cyclodepsipeptide of Marine Origin

Tsuyoshi Mutou, Kiyotake Suenaga, Tatsuya Fujita, Takashi Itoh, Noboru Takada, Kozue Hayamizu, Hideo Kigoshi, Kiyoyuki Yamada

研究成果: Article

34 引用 (Scopus)

抜粋

Aurilide (1), a novel cyclodepsipeptide isolated from the Japanese sea hare Dolabella auricularia, was enantioselectively synthesized, and the present result unambiguously confirmed its stereostructure. In addition, the cytotoxicity of 1 was evaluated by employing synthetic 1.

元の言語English
ページ(範囲)199-201
ページ数3
ジャーナルSynlett
1997
発行部数2
DOI
出版物ステータスPublished - 1997 1 1
外部発表Yes

ASJC Scopus subject areas

  • Organic Chemistry

フィンガープリント Enantioselective Synthesis of Aurilide, a Cytotoxic 26-Membered Cyclodepsipeptide of Marine Origin' の研究トピックを掘り下げます。これらはともに一意のフィンガープリントを構成します。

  • これを引用

    Mutou, T., Suenaga, K., Fujita, T., Itoh, T., Takada, N., Hayamizu, K., Kigoshi, H., & Yamada, K. (1997). Enantioselective Synthesis of Aurilide, a Cytotoxic 26-Membered Cyclodepsipeptide of Marine Origin. Synlett, 1997(2), 199-201. https://doi.org/10.1055/s-1997-753