2014年7月
Redox-Neutral Iron-Sulfur Promoted Transformation of 2-Nitrophenols and 2,6-Disubstituted p-Cresols into 2-Arylbenzoxazoles
SYNLETT
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- 巻
- 25
- 号
- 11
- 開始ページ
- 1565
- 終了ページ
- 1570
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1055/s-0033-1338995
- 出版者・発行元
- GEORG THIEME VERLAG KG
A catalyst based on iron and elemental sulfur has been shown to efficiently promote a redox-neutral reaction between 2-nitrophenols and 2,6-disubstituted p-cresols, allowing for the preparation of 2-arylbenzoxazoles in good yields. This synthetic methodology also affords high atom economy without the use of any external oxidizing and/or reducing reagents. This is the first redox-condensation reaction of 2-nitrophenols with 2,6-disubstituted p-cresols.
- リンク情報
- ID情報
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- DOI : 10.1055/s-0033-1338995
- ISSN : 0936-5214
- eISSN : 1437-2096
- Web of Science ID : WOS:000338110700021