Synthetic studies on oligomycins. Enantiospecific synthesis of the oligomycin B spiroketal portion and establishment of the absolute stereochemistry of oligomycin B

Masaya Nakata; Takashi Ishiyama; Youichi Hirose; Hiroshi Maruoka; Kuniaki Tatsuta

doi:10.1016/S0040-4039(00)61353-9

Synthetic studies on oligomycins. Enantiospecific synthesis of the oligomycin B spiroketal portion and establishment of the absolute stereochemistry of oligomycin B

Masaya Nakata, Takashi Ishiyama, Youichi Hirose, Hiroshi Maruoka, Kuniaki Tatsuta

研究成果: Article › 査読

12 被引用数 (Scopus)

抄録

The enantiospecific synthesis of the oligomycin B degradation product 2, corresponding to the C19-C34 spiroketal portion, has been achieved by sequential coupling of the C19-C21, C22-C27, and C28-C34 subunits, establishing the absolute stereochemistry of oligomycin B.

本文言語	English
ページ（範囲）	8439-8442
ページ数	4
ジャーナル	Tetrahedron Letters
巻	34
号	52
DOI	https://doi.org/10.1016/S0040-4039(00)61353-9
出版ステータス	Published - 1993
外部発表	はい

ASJC Scopus subject areas

生化学
創薬
有機化学

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10.1016/S0040-4039(00)61353-9

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引用スタイル

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AU - Hirose, Youichi

AU - Maruoka, Hiroshi

AU - Tatsuta, Kuniaki

PY - 1993

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