Molecules 1999, 4(10), 310-315; doi:10.3390/41000310
Article

Trimethylcyanosilane as a Convenient Reagent for the Preparation of Trimethylsilyl Enol Ethers of 1,3-Diketones

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Received: 22 August 1999; Accepted: 12 September 1999 / Published: 10 October 1999
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Trimethylsilyl enol ethers of 1,3-diketones are generated “in situ” or obtained in high isolated yield by the reaction of 1,3-diketones with trimethylcyanosilane in various solvents such as cyclohexane, hexane, benzene, methylene chloride, chloroform, carbon tetrachloride, and acetonitrile.
Keywords: Trimethylcyanosilane; Silylation; 1; 3-Diketones; Trimethylsilyl enol ethers
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MDPI and ACS Style

Zhuo, J.-C. Trimethylcyanosilane as a Convenient Reagent for the Preparation of Trimethylsilyl Enol Ethers of 1,3-Diketones. Molecules 1999, 4, 310-315.

AMA Style

Zhuo J-C. Trimethylcyanosilane as a Convenient Reagent for the Preparation of Trimethylsilyl Enol Ethers of 1,3-Diketones. Molecules. 1999; 4(10):310-315.

Chicago/Turabian Style

Zhuo, Jin-Cong. 1999. "Trimethylcyanosilane as a Convenient Reagent for the Preparation of Trimethylsilyl Enol Ethers of 1,3-Diketones." Molecules 4, no. 10: 310-315.

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