The alkylation of Silyl Enol Ethers with S<sub>N</sub>1-Unreactive Iodides in the Presence of Silver Trifluoroacetate

Article Article scientifique Lettre The alkylation of Silyl Enol Ethers with S<sub>N</sub>1-Unreactive Iodides in the Presence of Silver Trifluoroacetate eng 1992 author Jefford Charles 24934 author Sledeski Adam author Lelandais Patrick Jean 26646 author Boukouvalas John 22156 1855-1858 10.1016/S0040-4039(00)74160-8 0040-4039 https://linkinghub.elsevier.com/retrieve/pii/S0040403900741608 Silyl enol ethers can be effectively alkylated with primary n-alkyl iodides in the presence of silver trifluoro-acetate to give monoalkyl ketones. Moderate yields of monoalkyl ketones are obtained by alkylating silyl enol ethers with primary n-alkyl iodides in the presence of silver trifluoroacetate. Alkylalion n-alkyl iodide Silver trifluoroacetate Silyl enol ether Dewey 540 Swiss National Science Foundation 20-27'966.89 CH 36 Département de chimie organique 141 false Tetrahedron Letters 33 14 1608e882-d33b-432a-93d5-f9d0f7826874 Article (Published version) Restricted Jefford_TL_1992331855.pdf 2176557 application/pdf Vignette Public 1-s2.0-S0040403900741608-gr1.gif 2034 image/gif restrictedAccess Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

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The alkylation of Silyl Enol Ethers with S_N1-Unreactive Iodides in the Presence of Silver Trifluoroacetate	Tetrahedron Letters			1992	349	0

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Lelandais, Patrick Jean