2011年2月
Studies on Transition Metal-Catalyzed Addition Reaction of Oxygen-, Nitrogen-, and Carbon-Nucleophiles onto Olefins
JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN
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- 巻
- 69
- 号
- 2
- 開始ページ
- 118
- 終了ページ
- 128
- 記述言語
- 日本語
- 掲載種別
- 書評論文,書評,文献紹介等
- 出版者・発行元
- SOC SYNTHETIC ORGANIC CHEM JPN
The studies on transition metal-catalyzed addition reactions of carboxylic acids, alcohols, sulfon-amides, and 1,3-diketones onto olefins toward the development of olefin hydration using transition metal catalysts were described. Both intramolecular cyclizations and intermolecular additions successfully proceeded to give the corresponding adducts under mild condition. For example, 2-allylphenol was treated in the presence of 1 mol% of (Cp*RuCl2)(2)/4AgOTf in benzene at reflux to afford 2,3-dihydrobenzofuran in 95% yield. Ru-xantphos catalysts showed high catalytic activities on the addition of 2-phenylbenzoic acid, 2-phenylethanol, and tosylamide with 4-allylanisole to afford the corresponding addition products in 95%, 78%, and 78% yields, respectively.
- リンク情報
- ID情報
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- ISSN : 0037-9980
- Web of Science ID : WOS:000287566000003