Synthesis of Functionalized Tetracyanocyclopentadienides from Tetracyanothiophene and Sulfones
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- Takeo Sakai
- Faculty of Pharmacy, Meijo University, Tempaku-ku, Nagoya 468-8503, Japan
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- Shohei Seo
- Faculty of Pharmacy, Meijo University, Tempaku-ku, Nagoya 468-8503, Japan
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- Junpei Matsuoka
- Faculty of Pharmacy, Meijo University, Tempaku-ku, Nagoya 468-8503, Japan
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- Yuji Mori
- Faculty of Pharmacy, Meijo University, Tempaku-ku, Nagoya 468-8503, Japan
書誌事項
- 公開日
- 2013-10-16
- 資源種別
- journal article
- DOI
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- 10.1021/jo401946j
- 公開者
- American Chemical Society (ACS)
この論文をさがす
説明
Tetracyanothiophene and tetracyano-1,4-dithiin react with a leaving group substituted carbon nucleophile such as ethyl benzenesulfonylacetate to afford substituted tetracyanocyclopentadienyl sodium derivatives in moderate to high yields through a putative condensation and desulfurization pathway. Subsequent functional-group transformation reactions on the Cp anion ring provided various C5R(CN)4(-) derivatives.
収録刊行物
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- The Journal of Organic Chemistry
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The Journal of Organic Chemistry 78 (21), 10978-10985, 2013-10-16
American Chemical Society (ACS)