Synthesis and Diels-Alder reactions of 1,2-dimethylene[2.n]metacyclophanes

Takehiko Yamato; Shinpei Miyamoto; Tohru Hironaka; Yoshinori Miura

doi:10.1021/ol0483403

Synthesis and Diels-Alder reactions of 1,2-dimethylene[2.n]metacyclophanes

Takehiko Yamato
, Shinpei Miyamoto
, Tohru Hironaka
, Yoshinori Miura

中央分析センター

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

42 被引用数 (Scopus)

抄録

(Chemical Equation Presented) The Diels-Alder reaction of 1,2-dimethylene[2.n]MCPs (MCP = metacyclophane) with suitable dienophiles followed by aromatization and photoinduced or FeCl₃-induced transannular cyclization afforded phenanthrene-anellated polycyclic aromatic hydrocarbons, which were found to adopt helical chirality in the solid state.

本文言語	英語
ページ（範囲）	3-6
ページ数	4
ジャーナル	Organic letters
巻	7
号	1
DOI	https://doi.org/10.1021/ol0483403
出版ステータス	出版済み - 1月 6 2005

!!!All Science Journal Classification (ASJC) codes

生化学
物理化学および理論化学
有機化学

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10.1021/ol0483403

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title = "Synthesis and Diels-Alder reactions of 1,2-dimethylene[2.n]metacyclophanes",

abstract = "(Chemical Equation Presented) The Diels-Alder reaction of 1,2-dimethylene[2.n]MCPs (MCP = metacyclophane) with suitable dienophiles followed by aromatization and photoinduced or FeCl3-induced transannular cyclization afforded phenanthrene-anellated polycyclic aromatic hydrocarbons, which were found to adopt helical chirality in the solid state.",

author = "Takehiko Yamato and Shinpei Miyamoto and Tohru Hironaka and Yoshinori Miura",

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T1 - Synthesis and Diels-Alder reactions of 1,2-dimethylene[2.n]metacyclophanes

AU - Yamato, Takehiko

AU - Miyamoto, Shinpei

AU - Hironaka, Tohru

AU - Miura, Yoshinori

PY - 2005/1/6

Y1 - 2005/1/6

N2 - (Chemical Equation Presented) The Diels-Alder reaction of 1,2-dimethylene[2.n]MCPs (MCP = metacyclophane) with suitable dienophiles followed by aromatization and photoinduced or FeCl3-induced transannular cyclization afforded phenanthrene-anellated polycyclic aromatic hydrocarbons, which were found to adopt helical chirality in the solid state.

AB - (Chemical Equation Presented) The Diels-Alder reaction of 1,2-dimethylene[2.n]MCPs (MCP = metacyclophane) with suitable dienophiles followed by aromatization and photoinduced or FeCl3-induced transannular cyclization afforded phenanthrene-anellated polycyclic aromatic hydrocarbons, which were found to adopt helical chirality in the solid state.

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UR - https://www.scopus.com/pages/publications/12344317281#tab=citedBy

U2 - 10.1021/ol0483403

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Synthesis and Diels-Alder reactions of 1,2-dimethylene[2.n]metacyclophanes

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!!!All Science Journal Classification (ASJC) codes

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