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Vinylic tellurides as precursors in a stereoselective and convergent route to Z-enynes and Z-trisubstituted enediynesDOI: 10.1590/S0103-50532004000300004 Keywords: z-vinylic tellurides, z-enynes, z-enediynes, stereoselective synthesis, convergent route. Abstract: vinylic tellurides of z configuration are transformed into higher order z-vinyl cyanocuprates by transmetallation with higher order lithium dimethyl- or n-butyl(thienyl)cyanocuprates. reaction of the obtained z-vinyl cyanocuprates with zinc chloride gives presumably mixed zinc-copper species which react with bromoalkynes leading to enynes and enediynes with retention of the z double bond configuration.
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