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

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)199-201
Number of pages3
JournalSynlett
Volume1997
Issue number2
DOIs
Publication statusPublished - 1997 Jan 1
Externally publishedYes

ASJC Scopus subject areas

  • Organic Chemistry

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    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