Synthesis of 8-amino-(dihydrofuran-fused perhydrophenanthrene) via copper-mediated amination reaction

Kenji Sugimoto; Kosuke Tamura; Noaki Toyooka; Yuji Matsuya

doi:10.3987/COM-13-S(S)38

Synthesis of 8-amino-(dihydrofuran-fused perhydrophenanthrene) via copper-mediated amination reaction

Kenji Sugimoto, Kosuke Tamura, Noaki Toyooka, Yuji Matsuya^*

^*この論文の責任著者

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

2 被引用数 (Scopus)

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Introduction of nitrogen substituents on a highly functionalized dihydrofuran-fused perhydrophenanthrene (DF) core was examined. Acetamide functionality could be introduced on the DF by copper-mediated Buchwald-type coupling. On the other hand, installation of free amino group on a DF was established via an aryl azide under the copper-mediated condition reported by Helquist and co-workers.

本文言語	英語
ページ（範囲）	755-763
ページ数	9
ジャーナル	Heterocycles
巻	88
号	1
DOI	https://doi.org/10.3987/COM-13-S(S)38
出版ステータス	出版済み - 2014

ASJC Scopus 主題領域

分析化学
薬理学
有機化学

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10.3987/COM-13-S(S)38

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title = "Synthesis of 8-amino-(dihydrofuran-fused perhydrophenanthrene) via copper-mediated amination reaction",

abstract = "Introduction of nitrogen substituents on a highly functionalized dihydrofuran-fused perhydrophenanthrene (DF) core was examined. Acetamide functionality could be introduced on the DF by copper-mediated Buchwald-type coupling. On the other hand, installation of free amino group on a DF was established via an aryl azide under the copper-mediated condition reported by Helquist and co-workers.",

author = "Kenji Sugimoto and Kosuke Tamura and Noaki Toyooka and Yuji Matsuya",

note = "Publisher Copyright: {\textcopyright} 2014 The Japan Institute of Heterocyclic Chemistry.",

year = "2014",

doi = "10.3987/COM-13-S(S)38",

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T1 - Synthesis of 8-amino-(dihydrofuran-fused perhydrophenanthrene) via copper-mediated amination reaction

AU - Sugimoto, Kenji

AU - Tamura, Kosuke

AU - Toyooka, Noaki

AU - Matsuya, Yuji

PY - 2014

Y1 - 2014

N2 - Introduction of nitrogen substituents on a highly functionalized dihydrofuran-fused perhydrophenanthrene (DF) core was examined. Acetamide functionality could be introduced on the DF by copper-mediated Buchwald-type coupling. On the other hand, installation of free amino group on a DF was established via an aryl azide under the copper-mediated condition reported by Helquist and co-workers.

AB - Introduction of nitrogen substituents on a highly functionalized dihydrofuran-fused perhydrophenanthrene (DF) core was examined. Acetamide functionality could be introduced on the DF by copper-mediated Buchwald-type coupling. On the other hand, installation of free amino group on a DF was established via an aryl azide under the copper-mediated condition reported by Helquist and co-workers.

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DO - 10.3987/COM-13-S(S)38

M3 - 学術論文

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SN - 0385-5414

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Synthesis of 8-amino-(dihydrofuran-fused perhydrophenanthrene) via copper-mediated amination reaction

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