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An Effective Synthesis of a (Pyridin-3-yl)isoxazole via 1,3-Dipolar Cycloaddition Using ZnCl2: Synthesis of a (2-Aminopyridin-3-yl)isoxazole Derivative and Its Antifungal Activity
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- Tanaka Keigo
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Inoue Satoshi
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Murai Norio
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Shirotori Syuji
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Nakamoto Kazutaka
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Abe Shinya
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Horii Takaaki
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Miyazaki Mamiko
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Hata Katsura
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Watanabe Naoaki
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Asada Makoto
- Discovery Research Laboratories, Eisai Co., Ltd.
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- Matsukura Masayuki
- Discovery Research Laboratories, Eisai Co., Ltd.
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Description
We described a rare example of an effective isoxazole synthesis via a 1,3-dipolar cycloaddition using ZnCl2, which allowed us to synthesize novel (2-aminopyridin-3-yl)isoxazole derivatives effectively. In addition, these compounds demonstrated potent antifungal activity in vitro against both Candida albicans and Aspergillus fumigatus.
Journal
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- Chemistry Letters
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Chemistry Letters 39 (10), 1033-1035, 2010
The Chemical Society of Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390001204584304000
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- NII Article ID
- 10027185362
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- NII Book ID
- AA00603318
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- ISSN
- 13480715
- 03667022
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed