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Birgit Wieczorek Maarten R. Egmond Gerard van Koten 《Journal of organometallic chemistry》2009,694(6):812-2366
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J.W.F.L. Seetz F.A. Hartog H.P. Böhm C. Blomberg O.S. Akkerman F. Bickelhaupt 《Tetrahedron letters》1982,23(14):1497-1500
Careful addition of 1,3-dibromopropane to magnesium in Et2O yields 1,3-bis(bromomagnesio)propane which is purified via “magnesacyclobutane” . Reactions of with H2O, CO2, HgBr2 and Me3SnCl are reported. MgBr2 catalyses the decomposition of to allylmagnesium bromide . 相似文献
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The cyclometallated monohydrides (R H or Me) react with NaOPri/PriOH/H2 to give fluxional tetrahydrides, probably . These are highly fluxional having magnetically equivalent hydridic hydrogens, even at ---100°C. When treated with HBr, , gives and with CO it gives a mixture of complexes which are probably (2 isomers) and . When treated with ButNC this tetrahydride undergoes similar reactions but another (major) product is formed which appears to be binuclear and fluxional and is probably of type , with four bridging hydrogens. 相似文献
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Interaction of a compound of the type with sodium hydride results in the formation of the Na salt of the carbanion (where ArF represents a polyfluorinated group), which can enter into an intramolecular nucleophilic substitution reaction with the formation of the corresponding polyfluorinated carbocyclic compound. This reaction may serve as a general method for producing such compounds. 相似文献
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A.V. Fokin 《Journal of fluorine chemistry》1980,16(6):565-566
Chlorine fluorosulfonate adds exceptionally easy not only to various alkenes, perfluorobenzene, but to alkynes too The addition of peroxydisulfuryldifluoride to alkyl- and perfluoroalkyliodides leads to unstable adducts, which decompose with the formation of alkylfluorosulfonates and iodine fluorosulfonate; the latter was trapped with fluoroalkenes The use of ClOSO2F allows to substitute selectively for the fluorosulfonate group the chlorine atom in monochloroacetic acid esters as well as the fluorine atom in hexafluoroacetone N-fluoroimine ClOSO2F serves as an exceptionally active chlorinating reagent for fluorinated alcohols, nitrosocompounds, perfluoroacid amides and particularly for benzene The reaction of (OSO2F)2 with perfluoroacid amides leads to the corresponding N,N-bis(fluorosulfonate)amides, which easily rearrange into alkylfluorosulfonates The hypochlorites of fluorinated alcohols are stable enough and they, similarly to ClOSO2F, are able to add to alkenes, fluoroalkenes (but not to perfluoroisobutylene), bis(trifluoromethyl)ketene, trifluoromethylisocyanate and perfluoronitriles The fluorosulfonatoacetic acid esters are unstable at the ambient temperature, but they can be widely used in situ as a very effective alkylating reagents 相似文献
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François Mathey 《Tetrahedron letters》1979,20(20):1753-1756
1-Benzyl-3,4-dimethylphosphate - is converted into 2-phenyl-4,5-dimethyl-λ3-phosphorin - through 1,2-dihydro-λ5-phosphorines and . 相似文献
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James Howson Peter B. Hitchcock J. David Smith 《Journal of organometallic chemistry》2005,690(1):69-75
The lithium derivative (1) reacted with AlCl3 or Me2AlCl to give, respectively, the monomeric compounds (2a) and (2b). The product from reaction with commercially available GaBr3 was the analytically pure monomeric heterocycle (3), indicating that the starting halide had been partially hydrolysed before use. The reaction between 1 and commercially available InCl3 gave a homogenous white solid (4) with X = Cl (59%) or OH (41%). The X-ray crystal structures of 2a, 3, and 4 have been determined. 相似文献
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