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Other Coupling Reactions

Coupling of xanthene with P-keto esters catalysed by a combination of nickel and iron. [Pg.141]

Handbook of Functionalized Organometallics Applications in Synthesis, ed. P. Knochel, Wiley-VCH, Weinheim, 2005, voL 1 and 2. [Pg.143]

Murahashi, Science of Synthesis, Thieme Verlag, Stuttgart, 2004, vol. 19. [Pg.143]

Privileged Chiral Ligands and Catalysts, ed. Q.-L. Zhou, Wiley-VCH, Wein-heim, 2011. [Pg.144]

Efficient Preparations of Fluorine Compounds, ed. H. W. Roesky, Wiley, Hoboken, 2013. [Pg.144]


Other coupling reactions were also employed to prepare poly(arylene etherjs. Polymerization of bis(aryloxy) monomers was demonstrated to occur in the presence of an Fe(III) chloride catalyst via a cation radical mechanism (Scholl reaction).134 This reaction also involves carbon-carbon bond formation and has been used to prepare soluble poly(ether sulfone)s, poly(ether ketone)s, and aromatic polyethers. [Pg.347]

The stereospecific preparation of Z- ,/l-dill uorostyrenes was accomplished by Davis and Burton via modification of the Heinze methodology, as illustrated in equation 4937,38. The Z- /,/i -di II uorostyrenes could be readily converted to other synthons, such as E- /i-di -/ -iodostyrenes ( -FIC=CFPh) and -a, / -difluoro-/ -tributylstannanes (E-PhFC=CFSnBu3), by known literature reactions38, and which could be utilized as synthons in other coupling reactions. [Pg.725]

N2)Os-(NH3)4(CO)]4+ has also been prepared by the oxidative coupling of amine ligands (58). Other coupling reactions have been used to prepare trans,trans-[ (CH3CN)(NH3)4Os(N2)Os(NH3)4(NCCH3) ]5+ from [Osvi(NH3)4(N)] under UV/Vis irradiation in acetonitrile (269). [Pg.306]

The method illustrated here may be applicable to many other coupling reactions between terminally functionalized polypropylenes and monofunctional or difunctional living polymers, yielding well-defined block copolymers of AB or ABA types containing a polypropylene segment. [Pg.241]

Presumably these and other coupling reactions promoted by Sm11 compounds proceed through intermediates containing Sm—R bonds. [Pg.1122]

Cyclotrimerization and Other Coupling Reactions of Titana- and Zirconacycles on the Way to Carbocycles 1252... [Pg.1243]

As was the case in the other coupling reactions, nonphosphine-based catalysts have also been applied in amination chemistry. In particular, N-heterocyclic carbenes such as (9) have provided successful results for a wide variety of amination transformations. Similarly, catalysts based upon phosphinous acid ligands (e g. (11)) have also found success in the amination of aryl chloride substrates. ... [Pg.5655]

This bimolecular coupling is a structure-sensitive reaction, and it illustrates a key characteristic of metal oxides multiple coordinative unsaturation of surface metal cations may facilitate coupling of ligands in a manner similar to that for unsaturated metal complexes in solution. Examples of other coupling reactions... [Pg.414]

Other coupled reactions involving Cr(VI) have been discussed by Westheimer, Medalia, and Beattie and Haight. If a 1-equivalent reductant such as Fe(II) reacts with Cr(VI), the first step presumably involves the formation of Cr(V) ... [Pg.302]

An organometallic equivalent that opens epoxides is a hydrosilane, for example, MeaSiH, and carbon monoxide, catalyzed by dicobalt octacarbonyl See 10-55 for other coupling reactions with organosilanes. Silyl enol ethers react with epoxides in a related reaction, but a Lewis acid, such as TiCl4, is required. ... [Pg.621]

The first reaction is then called the coupled and the second the coupling reaction. Thermodynamic coupling thus allows the coupled reaction to proceed in a direction opposite to that dictated by its affinity. This is, however, only possible when there exist other coupling reactions which proceed at a sufficient rate. We shall come across this coupling in another form in the last volume of this work in the study of thermal diffusion in which diffusion plays a role analogous to the coupled reaction, while the thermal conductivity corresponds to the coupling reaction. [Pg.42]

Coupling reactions. The Suzuki coupling involving chloroarenes uses (dbajjPdj, /-BujP, and CsjCOj. For other coupling reactions (e.g., Stille coupling) good results are obtained in supercritical carbon dioxide. ... [Pg.418]

Other coupling reactions. A model study has demonstrated the utility of intramolecular Heck reaction in the construction of the morphine skeleton. It is surprising that only the desirable regioisomer is formed. [Pg.414]


See other pages where Other Coupling Reactions is mentioned: [Pg.534]    [Pg.547]    [Pg.79]    [Pg.116]    [Pg.291]    [Pg.3]    [Pg.4]    [Pg.17]    [Pg.108]    [Pg.153]    [Pg.449]    [Pg.362]    [Pg.1793]    [Pg.1828]    [Pg.2333]    [Pg.36]    [Pg.14]    [Pg.254]    [Pg.1340]    [Pg.4]    [Pg.23]    [Pg.255]    [Pg.5646]    [Pg.180]    [Pg.587]    [Pg.1342]    [Pg.1342]    [Pg.232]    [Pg.51]    [Pg.316]    [Pg.1340]    [Pg.10]    [Pg.242]    [Pg.470]   


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Esterifications using other coupling reactions

Heck Reactions Combined with Other Cross-Coupling Processes

Other Coupled Chemical Reactions

Other Cross-Coupling Reactions

Other Metal-Catalyzed Coupling Reactions

Other palladium-catalyzed cross-coupling reactions

Supported Palladium Catalysts in Other Coupling Reactions

The Heck Coupling in Combination with Other Reactions

Transmetallation to other Metals for Addition and Coupling Reactions

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