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The dichlorovinylation of enolates
Authors:Andrew S. Kende  Michel Benechie  Dennis P. Curran  Pawel Fludzinski  Wendy Swenson  Jon Clardy
Affiliation:Department of Chemistry, University of Rochester, Rochester, New York 14627 U.S.A.;Department of Chemistry, Cornell University, Ithaca, New York 14853 U.S.A.
Abstract:
The condensation of certain ketone and ester enolates with trichloroethylene proceeds with surprising ease to yield dichlorovinylation products. The trans stereochemistry for one such product is established by X-ray, and subsequent transformations of these initial products to ethinyl or ω-chloroethinyl derivatives is described.
Keywords:
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