Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid

Isao Shimizu; Tomoko Ishikawa

doi:10.1016/S0040-4039(00)73192-3

Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid

Isao Shimizu^*, Tomoko Ishikawa

^*この研究の対応する著者

早稲田大学

研究成果: Article › 査読

28 被引用数 (Scopus)

抄録

(±)-Clavukerin A and (±)-isoclavukerin A were synthesized stereoselectively utilizing stereospecific palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid.

本文言語	English
ページ（範囲）	1905-1908
ページ数	4
ジャーナル	Tetrahedron Letters
巻	35
号	12
DOI	https://doi.org/10.1016/S0040-4039(00)73192-3
出版ステータス	Published - 1994 3月 21

ASJC Scopus subject areas

生化学
有機化学
創薬

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10.1016/S0040-4039(00)73192-3

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「Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル

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abstract = "(±)-Clavukerin A and (±)-isoclavukerin A were synthesized stereoselectively utilizing stereospecific palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid.",

author = "Isao Shimizu and Tomoko Ishikawa",

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