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Carhene complexes

Cyclic Carhene Complexes. The reaction of aziridines with carbonyl, thiocarbonyl, or isonitrile ligands in Mn, Re, Fe, Ru, Pd, or Pt complexes leads to formation of cycHc carhene complexes (324—331). [Pg.10]

Minghetti, G., Bonati, F. and Banditelli, G. (1976) Carhene Complexes Of Gold (III) And Reactions Of Coordinated Ligand. Inorganic Chemistry, 15(7), 1718-1720. [Pg.178]

Synthetic Applications of Hetewatom-Suhstituted Carhene Complexes... [Pg.55]

Synthetic Applications of Non-Heteroatom-Substituted Carhene Complexes 117... [Pg.117]

Synthetic Applications of Acceptor-Substituted Carhene Complexes 181 Table 4.2. Intramolecular 1,2-C-H insertion of acceptor-substituted carbene complexes. [Pg.181]

Fig. 4.18. Possible mechanism of the olefination of thiocarbonyl compounds with electrophilic carhene complexes [1336]. Fig. 4.18. Possible mechanism of the olefination of thiocarbonyl compounds with electrophilic carhene complexes [1336].
Figure 3.3 Synthesis of a transition metal carhene complex with Ag-Au interactions. Figure 3.3 Synthesis of a transition metal carhene complex with Ag-Au interactions.
Figure 3.49 Synthesis of a dimeric palladium(ll) carhene complex featuring a chiral eimino functionalised NHC ligand. Figure 3.49 Synthesis of a dimeric palladium(ll) carhene complex featuring a chiral eimino functionalised NHC ligand.
Aryl ketones and esters. A Pd-carhene complex is useful for s3mthesis of heteroaryl ketones under CO. The couphng involving ArCHO in the air leads to aryl aroates. ... [Pg.322]

Exploration of metal-carhene complexes in catalysis for various reactions is in vogue. Perfomiing Heck reaction in the ionic liquid N-methyl-N -(2-diisopropylaminoethyl)imida-... [Pg.343]

Chromium carhene complexes, 82 Lthyl diazo(lithio)acctate. 230 Reformatsky rca tent, 348 Titanmm(lV) chloride, 304 By other reactions t>i i CarbonylhexaGaibonyldicobaU, 99... [Pg.397]

Cossee type. The mechanism comprised of olefin metathesis type elementary processes involving a metal carhene complex and a metallacyclobutane was established only recently after the development of the chemistry of metal-carbene complexes [129], Understanding of the novel kind of reaction mechanism opened a new horizon in polymerization. Various new types of polymerization of cyclic monomers have been realized by ROMP. An advantage of the process is that the processes are tolerant to polar reactants and solvents enabling ready incorporation of polar substituents into polymers. Another advantage is that the ROMP is living in nature and polymers of narrow molecular weight distributions are available by the method. [Pg.49]

Adihart, C. Hinderling, C. Baumann, H. Chen, P. Mechanistic Studies of Olefin Metathesis hy Ruthenium Carhene Complexes Using Electrospray Ionization Tandem Mass Spectrometry. J. Am. Chem. Soc. 2000,122, 8204-8214. [Pg.215]


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See also in sourсe #XX -- [ Pg.65 , Pg.657 , Pg.658 , Pg.659 , Pg.660 , Pg.661 ]




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