A new synthetic method for the preparation of di-μ-chlorobis[π-1-chloro-1-aryl-2-(2′,2′-diarylvinyl)allyl]palladium(II) complexes has been developed from the reaction of arylvinylcyclopropenes with a Pd(II) complex along with a novel dehydrogenative rearrangement of arylvinylcyclopropenes via di-μ-chlorobis[π-1-chloro-1-aryl-2-(2′,2′-diarylvinyl)allyl]palladium(II) complexes to produce 7 H -benzo[ c ]fluorene derivatives in good yields under mild conditions. A stoichiometric amount of silver salts or a catalytic amount of strong Brønsted acid HOTf can be the promoter or the catalyst for this interesting dehydrogenative rearrangement.
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Zhu et al. (2011) studied this question.
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