Journal
ORGANOMETALLICS
Volume 30, Issue 3, Pages 627-632Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om1009846
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Funding
- Shanghai Municipal Committee of Science and Technology [08dj1400100-2]
- National Basic Research Program of China (973) [2009CB825300]
- Fundamental Research Funds for the Central Universities
- National Natural Science Foundation of China [20472096, 20872162, 20672127, 20821002, 20732008]
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A new synthetic method for the preparation of di-mu-chlorobis[pi-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-mu-chlorobis-[pi-1-chloro-1-aryl-2-(2',2'-diarylvinyl)allyl]palladium(II) complexes to produce 7H-benzo[c]fluorene derivatives in good yields under mild conditions. A stoichiometric amount of silver salts or a catalytic amount of strong Bronsted acid HOTf can be the promoter or the catalyst for this interesting dehydrogenative rearrangement.
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