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Vinylic tellurides as precursors in a stereoselective and convergent route to Z-enynes and Z-trisubstituted enediynes

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.

Z-Vinylic tellurides; Z-enynes; Z-enediynes; stereoselective synthesis; convergent route


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