The first total synthesis and structural determination of actinopyrone A

Seijiro Hosokawa; Kazuya Yokota; Keisuke Imamura; Yasuaki Suzuki; Masataka Kawarasaki; Kuniaki Tatsuta

doi:10.1016/j.tetlet.2006.05.028

The first total synthesis and structural determination of actinopyrone A

Seijiro Hosokawa, Kazuya Yokota, Keisuke Imamura, Yasuaki Suzuki, Masataka Kawarasaki, Kuniaki Tatsuta

先進理工学部

研究成果: Article › 査読

36 被引用数 (Scopus)

抄録

Actinopyrone A (1) has been synthesized by using our developed remote stereoinduction, Kocienski olefination, Horner-Wadsworth-Emmons olefination, and reductive de-conjugation of the vinylpyrone. A concise method of O-methylation to obtain the γ-pyrone has also been established.

本文言語	English
ページ（範囲）	5415-5418
ページ数	4
ジャーナル	Tetrahedron Letters
巻	47
号	30
DOI	https://doi.org/10.1016/j.tetlet.2006.05.028
出版ステータス	Published - 2006 7 24

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

文献へのアクセス

10.1016/j.tetlet.2006.05.028

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引用スタイル

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AU - Hosokawa, Seijiro

AU - Yokota, Kazuya

AU - Imamura, Keisuke

AU - Suzuki, Yasuaki

AU - Kawarasaki, Masataka

AU - Tatsuta, Kuniaki

PY - 2006/7/24

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KW - 4-Pyrone

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KW - Reductive de-conjugation

KW - Remote stereoinduction

KW - Structural determination

KW - Total synthesis

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