Alkylation of Phenols by Oxidation-Reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone and Alkoxydiphenylphosphine
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概要
- 論文の詳細を見る
- 2003-01-05
著者
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Shintou T
Kitasato Inst. Tokyo
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KIKUCHI Wataru
Center for Basic Research, Kitasato Institute
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SHINTOU Taichi
The Kitasato Institute, Center for Basic Research
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KIKUCHI Wataru
The Kitasato Institute, Center for Basic Research
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Kikuchi Wataru
Center For Basic Research Kitasato Institute
関連論文
- An Efficient Method for the p-Methoxybenzylation of Hydroxy Groups with 2-(4-Methoxybenzyloxy)-3-nitropyridine
- Efficient Method for the Preparation of Carboxylic Acid Alkyl Esters or Alkyl Phenyl Ethers by a New-Type of Oxidation-Reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone and Alkoxydiphenylphosphines
- New One-pot Cross-coupling Reaction between Grignard Reagents and Alkoxymethyldiphenylphosphonium Iodides in situ-Formed from Alcohols, Chlorodiphenylphosphine and Iodomethane
- Preparation of Various Carboxylic Acid Esters from Bulky Alcohols and Carboxylic Acids by a New Type Oxidation-reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone
- Alkylation of Phenols by Oxidation-Reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone and Alkoxydiphenylphosphine
- Benzylation of Carboxylic Acids by Oxidation-Reduction Condensation Using Quinones and Benzyloxydiphenylphosphine
- Lithium Tetrakis(pentafluorophenyl)borate-Catalyzed Friedel-Crafts Benzylation Reactions