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For some selected papers, see:
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In: Diederich F., and Stang P.J. (Eds). Metal-Catalyzed Cross-Coupling Reactions (1998), Wiley, New York, NY
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20544450502
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de Meijere A., and Diederich F. (Eds), Wiley, Weinheim, Germany
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In: de Meijere A., and Diederich F. (Eds). Metal-Catalyzed Cross-Coupling Reactions. 2nd ed. Vol. 2 (2004), Wiley, Weinheim, Germany
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35348852942
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For selected reviews and papers, see:
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0000509322
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Chapter 2.4. Trost B.M., and Fleming I. (Eds), Pergamon, Oxford and references cited therein
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Sonogashira K. Chapter 2.4. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 3 (1991), Pergamon, Oxford 521 and references cited therein
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Sonogashira, K.1
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35348904749
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For some recent selected papers, see:
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35348817718
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For some selected papers, see:
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35348872868
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For some selected papers, see:
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Thathagar M.B., Beckers J., and Rothenberg G. Green Chem. 6 (2004) 215-218 For copper-catalyzed cross-coupling reactions, see:
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35348907636
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For copper-catalyzed coupling reaction of alkenyl halides with alkynes in the presence of ligands, see:
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26844534413
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For other transformations of the diiodides from this group, see:
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Shao L.-X., and Shi M. J. Org. Chem. 70 (2005) 8635-8637 For other transformations of the diiodides from this group, see:
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For the stoichiometric amount of copper-catalyzed coupling reactions of carbon-heteroatom bond in the absence of palladium and ligand, see:
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For the stoichiometric amount of copper-catalyzed coupling reactions of carbon-heteroatom bond in the absence of palladium and ligand, see:. Commercon A., Normant J., and Villieras J. J. Organomet. Chem. 93 (1975) 415-421
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55
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35348824663
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-
note
-
2NH as the base and solvent (see Ref. 11a). Although for the various amines screened, some of which showed excellent results for the coupling reaction, the reproducibility is very poor in the presence of organic bases.
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