Studies toward the synthesis of perforatumone: Synthesis of the 7-OXABICYCLO[4.2.1]NONANE-8,9-DIONE CORE

Tatsuki Nakajima; Keita Takiguchi; Keisuke Yoshida; Akihiro Ogura; Ken Ichi Takao

doi:10.3987/COM-18-S(F)31

Studies toward the synthesis of perforatumone: Synthesis of the 7-OXABICYCLO[4.2.1]NONANE-8,9-DIONE CORE

Tatsuki Nakajima
, Keita Takiguchi
, Keisuke Yoshida
, Akihiro Ogura
, Ken Ichi Takao

応用化学科

研究成果: Article › 査読

1 被引用数 (Scopus)

抄録

Construction of the unique bridged bicyclic skeleton, 7-oxabicyclo[4.2.1]nonane-8,9-dione, of perforatumone was achieved. Key steps included a Dieckmann-type condensation, a Claisen rearrangement, and an intramolecular Michael reaction.

本文言語	English
ページ（範囲）	661-668
ページ数	8
ジャーナル	Heterocycles
巻	99
号	1
DOI	https://doi.org/10.3987/COM-18-S(F)31
出版ステータス	Published - 2019

ASJC Scopus subject areas

分析化学
薬理学
有機化学

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10.3987/COM-18-S(F)31

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title = "Studies toward the synthesis of perforatumone: Synthesis of the 7-OXABICYCLO[4.2.1]NONANE-8,9-DIONE CORE",

abstract = "Construction of the unique bridged bicyclic skeleton, 7-oxabicyclo[4.2.1]nonane-8,9-dione, of perforatumone was achieved. Key steps included a Dieckmann-type condensation, a Claisen rearrangement, and an intramolecular Michael reaction.",

author = "Tatsuki Nakajima and Keita Takiguchi and Keisuke Yoshida and Akihiro Ogura and Takao, \{Ken Ichi\}",

note = "Publisher Copyright: {\textcopyright} 2019 The Japan Institute of Heterocyclic Chemistry.",

year = "2019",

doi = "10.3987/COM-18-S(F)31",

language = "English",

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AU - Nakajima, Tatsuki

AU - Takiguchi, Keita

AU - Yoshida, Keisuke

AU - Ogura, Akihiro

AU - Takao, Ken Ichi

PY - 2019

Y1 - 2019

N2 - Construction of the unique bridged bicyclic skeleton, 7-oxabicyclo[4.2.1]nonane-8,9-dione, of perforatumone was achieved. Key steps included a Dieckmann-type condensation, a Claisen rearrangement, and an intramolecular Michael reaction.

AB - Construction of the unique bridged bicyclic skeleton, 7-oxabicyclo[4.2.1]nonane-8,9-dione, of perforatumone was achieved. Key steps included a Dieckmann-type condensation, a Claisen rearrangement, and an intramolecular Michael reaction.

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UR - https://www.scopus.com/pages/publications/85069639904#tab=citedBy

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DO - 10.3987/COM-18-S(F)31

M3 - Article

AN - SCOPUS:85069639904

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Studies toward the synthesis of perforatumone: Synthesis of the 7-OXABICYCLO[4.2.1]NONANE-8,9-DIONE CORE

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