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https://doi.org/10.1002/cber.19941270311
Copy DOIJournal: Chemische Berichte | Publication Date: Mar 1, 1994 |
Citations: 17 | License type: other-oa |
AbstractRelative reactivities of alkenes and alkynes toward diarylmethyl cations have been determined by direct rate measurements and by competition experiments in dichloromethane. At −70°C alkynes are found to be one to two orders of magnitude less reactive than analogously substituted alkenes (e.g. phenylacetylene/styrene), but the reactivity difference reduces strongly as the temperature is raised. The stereochemistry of the vinyl chlorides produced by addition of benzhydryl chlorides to alkynes is characterized.
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