Rhodium-Catalyzed Activation and Functionalization of the C−C Bond of Biphenylene
Author:
Affiliation:
1. Department of Chemistry, University of Rochester, Rochester, New York 14627
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om0107946
Reference32 articles.
1. Recent reviews highlight C−C bond activation: (a) Murakami, M.; Ito, Y. InTopics in Organometallic Chemistry; Murai, S., Ed.; Springer-Verlag: New York, 1999; Vol. 3, pp 96−129. (b) Rybtchinski, B.; Milstein, D.Angew.Chem., Int. Ed.1999,38, 871.
2. Catalytic Carbon−Carbon and Carbon−Hydrogen Bond Cleavage in Lower Alkanes. Low-Temperature Hydroxylations and Hydroxycarbonylations with Dioxygen as the Oxidant
3. Oxidative addition of quadricyclene to di-µ-chlorotetracarbonyldirhodium(I) and the mechanism of the rhodium(I)-catalysed isomerization of quadricyclene to norbornadiene
4. Catalysis of symmetry-restricted reactions by transition metal compounds. Valence isomerization of cubane
5. Interaction of rhodium(I) with cyclopropenones: decarbonylation and formation of 1-rhodacyclopentene-2,5-diones and cationic oxygen .sigma.-bound cyclopropenone complexes. X-ray crystal structure of trans-carbonylbis(triphenylphosphine)(di-tert-butylcyclopropenone)rhodium trifluoromethanesulfonate
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