Abstract
Trimethylsilyldiazomethane reacts smoothly with phenols and enols in methanolic acetonitrile solution in the presence of N, N-diisopropylethylamine to give methyl ethers. © 1984, The Pharmaceutical Society of Japan. All rights reserved.
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APA
Aoyama, T., Terasawa, S., Sudo, K., & Shioiri, T. (1984). New Methods and Reagents in Organic Synthesis. 46. Trimethylsilyldiazomethane: A Convenient Reagent for the O-Methylation of Phenols and Enols. Chemical and Pharmaceutical Bulletin, 32(9), 3759–3760. https://doi.org/10.1248/cpb.32.3759
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