Selective Intermolecular [2+2+2] Cycloaddition of Terminal Alkynes and Alkenes by NbCl5 as a Catalyst Precursor
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- Kamei Motofumi
- Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University
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- Watanabe Keisuke
- Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University
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- Fuji Maito
- Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University
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- Obora Yasushi
- Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University
書誌事項
- タイトル別名
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- Selective Intermolecular [2+2+2] Cycloaddition of Terminal Alkynes and Alkenes by NbCl<sub>5</sub> as a Catalyst Precursor
抄録
NbCl5 serves as an efficient catalyst for the intermolecular [2+2+2] cycloaddition of alkynes and alkenes to afford 1,3-cyclohexadienes. A convenient system has been developed using excess alkene, which enables the reaction to proceed without using low-valent niobium reagents or any reductants. This catalytic system affords 1,3-cyclohexadiene with high chemo- and regioselectivity, in contrast to a previously reported system involving NbCl3(DME) as a low-valent niobium catalyst.
収録刊行物
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- Chemistry Letters
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Chemistry Letters 45 (8), 943-945, 2016
公益社団法人 日本化学会
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詳細情報 詳細情報について
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- CRID
- 1390282679564727168
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- NII論文ID
- 130005254631
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- ISSN
- 13480715
- 03667022
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可