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

doi:10.1055/s-1997-753

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 journal › Article › peer-review

35 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 language	English
Pages (from-to)	199-201
Number of pages	3
Journal	Synlett
Volume	1997
Issue number	2
DOIs	https://doi.org/10.1055/s-1997-753
Publication status	Published - 1997 Jan 1
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1055/s-1997-753

Cite this

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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.",

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

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T1 - Enantioselective Synthesis of Aurilide, a Cytotoxic 26-Membered Cyclodepsipeptide of Marine Origin

AU - Mutou, Tsuyoshi

AU - Suenaga, Kiyotake

AU - Fujita, Tatsuya

AU - Itoh, Takashi

AU - Takada, Noboru

AU - Hayamizu, Kozue

AU - Kigoshi, Hideo

AU - Yamada, Kiyoyuki

PY - 1997/1/1

Y1 - 1997/1/1

N2 - 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.

AB - 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.

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DO - 10.1055/s-1997-753

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

Abstract

ASJC Scopus subject areas

UN SDGs

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