A facile preparation of functional cycloalkynes <i>via</i> an azide-to-cycloalkyne switching approach
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- Suguru Yoshida
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
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- Tomoko Kuribara
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
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- Harumi Ito
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
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- Tomohiro Meguro
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
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- Yoshitake Nishiyama
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
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- Fumika Karaki
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
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- Yasutomo Hatakeyama
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
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- Yuka Koike
- Common Facilities Unit
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- Isao Kii
- Laboratory for Pathophysiological and Health Science
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- Takamitsu Hosoya
- Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering
書誌事項
- 公開日
- 2019
- 資源種別
- journal article
- 権利情報
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- http://creativecommons.org/licenses/by/3.0/
- DOI
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- 10.1039/c9cc01113g
- 公開者
- Royal Society of Chemistry (RSC)
この論文をさがす
説明
<p>Terminal alkyne-selective click conjugation of diynes bearing strained and terminal alkyne moieties with functional azides has been achieved by transient protection of strained alkynes <italic>via</italic> complexation with copper to easily afford various functional cycloalkynes.</p>
収録刊行物
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- Chemical Communications
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Chemical Communications 55 (24), 3556-3559, 2019
Royal Society of Chemistry (RSC)
